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Showing posts with label TERPENOIDS. Show all posts
Showing posts with label TERPENOIDS. Show all posts

1 Benzoin-Synonyms Bitter-almond-oil camphor

4. Benzoin

Synonyms Bitter-almond-oil camphor.
Biological Source Benzoin in the balsamic resin obtained from Styrax benzoin Dryander and Styrax paralleloneurus Perkins, generally known in trade as Sumatra Benzoin; whereas, Styrax tonkinensis (Pierre) Craib ex Hartwich, or other species of the section Anthostyrax of the genus Styrax, known commonly in the trade as Siam Benzoin both belong to the family: Styraceae.
Preparation Benzoin is also a pathological product that is obtained by incising a deep-cut in the bark. It has been observed that after a span of about eight weeks, the exudating balsamic resin tends to become less sticky in nature and firm enough to collect. The entire exudate is usually collected in two stages, namely:
Stage 1: First tapping-yields almond tears, and
Stage 2: Second tapping-yields a more fluid material.
Characteristic Features
Sumatra Benzoin: It is pertinent to mention here that in pharmacy, only the Sumatra Benzoin is used. It occurs as blocks or irregular masses of tears having variable sizes usually imbedded either in an opaque or translucent matrix. It is rather brittle, and from within the tears are milky white in appearance. It generally becomes soft when warmed and gritty when chewed. The matrix is grayish brown to reddish in colour. Its taste is quite agreeable, balsamic and resembles to that of storax. It has a resinous and aromatic taste.
Siam Benzoin: The smaller tears of Siam Benzoin are darker in colour. It occurs largely in separate concavo-convex tears which are yellowish brown to rusty brown externally, whereas milky white internally. The tears are fairly brittle but normally become soft and plastic like on being chewed. It has a vanilla-like fragrance.
Chemical Constituents The chemical constituents of the two types of Benzoin are given below:
(a) Sumatra Benzoin: It contains free balsamic acids, largely cinnamic acid (10%), benzoic acid (6%)-along with their corresponding ester derivatives. Besides, it also contains teriterpene acids, namely: 19-hydroxyloleanolic and 6-hydroxyoleanolic acids, cinnamyl cinnamate, phenyl propyl cinnamate, phenylethylene and lastly the traces of vanillin. It yields not less than 75% of alccohol-soluble extractives.
(b) Siam Benzoin: It chiefly comprises of coniferyl benzoate (60-70%), benzoic acid (10%), triterpene siaresinol (6%) and traces of vanillin. It yields not less than 90% of alcoholsoluble extractives.

coniferyl benzoate
Chemical Tests
1. When 0.5 g of Sumatra Benzoin powder is warmed with 10 ml of KMnO4 solution (5% w/v) in a test tube, a faint and distinct odour of benzaldehyde is developed. Siam Benzoin gives a negative test.
2. When 0.2 g of Siam Benzoin powder is digested with 5 ml of ether for 5 minutes and filtered; 1 ml of the filtrate is poured into a clean china-dish containing 2-3 drops of concentrated H2SO4 and mixed carefully, a deep purplish red colouration is developed instantly. Sumatra Benzoin gives a negative test.
Uses
1. Compound benzoin tincture is frequently employed as a topical protectant.
2. It is valuable as an expectorant when vapourized.
3. It finds its usage as a cosmetic lotion usually prepared from a simple tincture.
4. Siam Benzoin has been proved to be a better preservative for lard than the Sumatra Benzoin.

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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0 Tolu Balsam-Synonyms Thomas balsam; Opobalsam; Resin Tolu; Balsam of Tolu

3. Tolu Balsam


Synonyms Thomas balsam; Opobalsam; Resin Tolu; Balsam of Tolu.
Biological Source Tolu Balsam is a balsam obtained from Toluifera balsamum L., (Myroxylon toluiferum H.B.K.), belonging to family: Leguminosae. It is also obtained from Myroxylon balsamum (Linne') Harms. Family: Fabaceae.
Preparation Tolu Balsam is considered to be a pathological product produced in the new wood formed as a result of inflicted injury. For its preparation, it is an usual practice to make ‘V’ shaped incisions deep into the body of the main trunk. The exudate thus produced is collected either in cups or gourds held strategically just at the base of each incisions. Balsam of Tolu is collected from these cups, mixed and packed in air-tight sealed tins.
Characteristic Features It is a yellowish-brown or brown semifluid or nearly solid resinous mass. It has a characteristic aromatic vanilla-like odour and slightly pungent taste. It is usually brittle when cold. It is found to be transparent in thin layers, and shows numerous crystals of cinnamic acid. It is almost insoluble in water and petroleum ether, but freely soluble in ethanol, benzene chloroform, ether, glacial acetic acid and partially in CS2 or NaOH solution.
Chemical Constituents The drug contains resin esters (75-80%) viz., toluresinotannol cinnamate along with a small proportion of the benzoate; volatile oil (7-8%)-containing chiefly benzyl benzoate; free cinnamic acid (12-15%); free benzoic acid (2-8%); vanillin and other constituents in small quantities. It also contains cinnamein (5-13%).
Chemical Tests
1. An alcoholic solution of Tolu Balsam (0.2% w/v) where treated with a FeCl3 solution (0.5% w/v), the appearances of a green colour takes place.
2. Treatment of 1 g of the drug with 5 ml of 10% w/v KMnO4 solution when subjected to gentle heating yields benzaldehyde.
Uses
1. It is used extensively in perfumery, confectionery and chewing gums.
2. It is used widely as an expectorant in cough mixture.
3. It also finds its application as an antiseptic in the form of its tincture.

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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0 Peruvian Balsam-Synonyms Balsam Peru; Indian balsam; Black balsam; China oil; Honduras balsam; Surinam balsam

2. Peruvian Balsam

Synonyms Balsam Peru; Indian balsam; Black balsam; China oil; Honduras balsam; Surinam balsam.
Biological Source Balsam Peru is obtained from Toluifer pereiare (Klotzsch) Baill. (Myroxylon pereiare Klotzsch) belonging to family: Leguminosae.
Preparation Peruvian Balsam is a pathological product and is obtained usually by inflicting injury to the trees. Most of the world's commercial supply comes from El Salvador, although some is also produced in Honduras.
It is prepared by beating the stems of the trees with mallet. After a week the injured areas of the stem are scorched so as to separate the bark from the stem and after a similar duration the bark is peeled off completely. The desired balsam starts exuding freely from all the exposed surfaces, which are then covered carefully with cloth or rags to absorb the exuding balsam. The cloth or rags that are completely soaked with the balsam is then removed and boiled with water in a large vessel slowly.
Thus, the balsam gets separated and settles at the bottom of the vessel. The supernatant layer of water is removed by decantation and the residual balsam is dried and packed in the containers.
Characteristic Features It is a dark brown, viscid liquid having a pleasant aromatic odour. It has a peculiar warm bitter taste and persistent aftertaste which resembles like vanilla. The Balsam Peru is transparent in thin films. It does not harden on being exposed to atmosphere. It is brittle when cold. It is almost insoluble in water and petroleum ether but soluble in ethanol, chloroform and glacial acetic acid.
Chemical Constituents Peruvian balsam contains free benzoic and cinnamic acids (12-15%); benzyl (40%); esters of these acids (5.2-13.4% cinnamein); and volatile oil (1.5-3%).
The fragrant volatile oil contains toluene, styrol, benzoic and cinnamic acids.
It also contains total balsamic acids, which is calculated on the basis of dry alcohol-soluble matter ranging between (35-50%).

cinnamein
The resins esters (30-38%) are chiefly composed of peruresinotannol cinnamate and benzoate, vanillin, free cinnamic acid and peruviol (or nerolidol).

peruviol (or nerolidol)
Uses
1. Peru balsam is a local protectant and rubefacient.
2. It also serves as a parasiticide in certain skin disorder.
3. It is used as an antiseptic and vulnerary* and is applied externally either as ointment or alone or in alcoholic solution.
4. It acts as an astringent to treat hemorrhoids.
------------------------------------------------
* Vulnerary: A folk remedy or herb to promote wound healing.

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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0 Balsams-Synonyms Styrax; Sweet oriental gum; Levant Storax; Purified or prepared Storax; American Storax; Liquid Storax

1. Storax

Synonyms Styrax; Sweet oriental gum; Levant Storax; Purified or prepared Storax; American Storax; Liquid Storax;
Biological Source Storax is the balsam obtained from the trunk of Liquidamber orientalis Mill., termed as Levant Storax, or of L. styraciflua L., known as American Storax belonging to the natural order Hamamelidaceae.
Preparation The natural balsam storax is a pathological product formed as a result of injury caused to the plant. It generally, exudes into the natural pockets between the bark and the wood and may be located by exerscences on the outerside of the bark. These pockets, that may contain upto 4 kg of the balsam, are conveniently tapped with the help of strategically positioned gutters, and the product is ultimately allowed to fill into containers. The crude storax, thus collected, is further purified by dissolving in ethanol, filtration and subsequent evaporation of the solvent to obtain the pure storax.
Characteristic Features The balsam storax is a semiliquid grayish, sticky, opaque mass (Levant Storax), or a semisolid sometimes solid mass softened by gentle warming (American Storax). In general, storax is transparent in thin layers, possesses a characteristic agreeable balsamic taste and odour. It is, however, denser than water. It is almost insoluble in water, but completely soluble in 1 part of warm ethanol, ether, acetone and CS2.
Chemical Constituents Storax contains the following chemical compounds, namely: α-and β-storesin and its cinnamic ester (30-50%), styracin (5-10%); phenylpropyl cinnamate (10%); free-cinnamic acid (5-15%); levorotatory oil (0.4%); small amounts of ethyl cinnamate, benzyl cinnamate, traces of vanillin and styrene (C6H5CH=CH2).
Besides, Levant storax contains free storesinol, isocinnamic acid, ethylvanillin, styrogenin, and styrocamphene.
In addition to these, American Storax contains styaresin (i.e., -cinnamic acid ester of the alcohol styresinol, an isomer of storesinol) and styresinolic acid. It also yields upto 7% of a dextrorotatony volatile oil, styrol and traces of vanillin.
Chemical Tests
1. Benzaldehyde Test—Treat 1 g of storax with 5 ml of K2Cr2O7 solution (10% w/v) followed by a few drops of concentrated sulphuric acid (36 N) it produces benzaldehyde, which may be detected easily as the odour of bitter almonds.
2. Mix 1g of storax with 3 g of pure sand (SiO2) and 5 ml of KMnO4 solution (5% w/v) and heat it gently. It gives a distinct odour of benzaldehyde.
Uses
1. It is used in fumigating pastilles and powders.
2. It finds its application in perfumery.
3. It is employed as an imbedding material in microscopy.
4. It is used as an expectorant, antiseptic and stimulant.
5. It is employed as a preservative for fatty substances e.g., lard and tallow.
6. It is also used as a flavouring agent for tobacco.
7. It is a vital ingredient of “Compound Benzoin Tincture”.

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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0 Balsams (Storax; Peruvain Balsam; Tolu Balsam; and Benzoin)

2.10 Balsams

Balsams are the resinous mixtures that essentially contain large quantum of benoic acid, cinnamic acid or both, or esters of these organic aromatic acids.
A galaxy of typical examples of naturally occurring balsams will be discussed in the sections that follow, namely: Storax; Peruvain Balsam; Tolu Balsam; and Benzoin.

1. Storax

Synonyms Styrax; Sweet oriental gum; Levant Storax; Purified or prepared Storax; American Storax; Liquid Storax;
Biological Source Storax is the balsam obtained from the trunk of Liquidamber orientalis Mill., termed as Levant Storax, or of L. styraciflua L., known as American Storax belonging to the natural order Hamamelidaceae.
Preparation The natural balsam storax is a pathological product formed as a result of injury caused to the plant. It generally, exudes into the natural pockets between the bark and the wood and may be located by exerscences on the outerside of the bark. These pockets, that may contain upto 4 kg of the balsam, are conveniently tapped with the help of strategically positioned gutters, and the product is ultimately allowed to fill into containers. The crude storax, thus collected, is further purified by dissolving in ethanol, filtration and subsequent evaporation of the solvent to obtain the pure storax.
Characteristic Features The balsam storax is a semiliquid grayish, sticky, opaque mass (Levant Storax), or a semisolid sometimes solid mass softened by gentle warming (American Storax). In general, storax is transparent in thin layers, possesses a characteristic agreeable balsamic taste and odour. It is, however, denser than water. It is almost insoluble in water, but completely soluble in 1 part of warm ethanol, ether, acetone and CS2.
Chemical Constituents Storax contains the following chemical compounds, namely: α-and β-storesin and its cinnamic ester (30-50%), styracin (5-10%); phenylpropyl cinnamate (10%); free-cinnamic acid (5-15%); levorotatory oil (0.4%); small amounts of ethyl cinnamate, benzyl cinnamate, traces of vanillin and styrene ( (C6H5CH=CH2).
Besides, Levant storax contains free storesinol, isocinnamic acid, ethylvanillin, styrogenin, and styrocamphene.
In addition to these, American Storax contains styaresin (i.e., -cinnamic acid ester of the alcohol styresinol, an isomer of storesinol) and styresinolic acid. It also yields upto 7% of a dextrorotatony volatile oil, styrol and traces of vanillin.
Chemical Tests
1. Benzaldehyde Test—Treat 1 g of storax with 5 ml of K2Cr2O7 solution (10% w/v) followed by a few drops of concentrated sulphuric acid (36 N) it produces benzaldehyde, which may be detected easily as the odour of bitter almonds.
2. Mix 1g of storax with 3 g of pure sand (SiO2) and 5 ml of KMnO4 solution (5% w/v) and heat it gently. It gives a distinct odour of benzaldehyde.
Uses
1. It is used in fumigating pastilles and powders.
2. It finds its application in perfumery.
3. It is employed as an imbedding material in microscopy.
4. It is used as an expectorant, antiseptic and stimulant.
5. It is employed as a preservative for fatty substances e.g., lard and tallow.
6. It is also used as a flavouring agent for tobacco.
7. It is a vital ingredient of “Compound Benzoin Tincture”.

2. Peruvian Balsam

Synonyms Balsam Peru; Indian balsam; Black balsam; China oil; Honduras balsam; Surinam balsam.
Biological Source Balsam Peru is obtained from Toluifer pereiare (Klotzsch) Baill. (Myroxylon pereiare Klotzsch) belonging to family: Leguminosae.
Preparation Peruvian Balsam is a pathological product and is obtained usually by inflicting injury to the trees. Most of the world's commercial supply comes from El Salvador, although some is also produced in Honduras.
It is prepared by beating the stems of the trees with mallet. After a week the injured areas of the stem are scorched so as to separate the bark from the stem and after a similar duration the bark is peeled off completely. The desired balsam starts exuding freely from all the exposed surfaces, which are then covered carefully with cloth or rags to absorb the exuding balsam. The cloth or rags that are completely soaked with the balsam is then removed and boiled with water in a large vessel slowly.
Thus, the balsam gets separated and settles at the bottom of the vessel. The supernatant layer of water is removed by decantation and the residual balsam is dried and packed in the containers.
Characteristic Features It is a dark brown, viscid liquid having a pleasant aromatic odour. It has a peculiar warm bitter taste and persistent aftertaste which resembles like vanilla. The Balsam Peru is transparent in thin films. It does not harden on being exposed to atmosphere. It is brittle when cold. It is almost insoluble in water and petroleum ether but soluble in ethanol, chloroform and glacial acetic acid.
Chemical Constituents Peruvian balsam contains free benzoic and cinnamic acids (12-15%); benzyl (40%); esters of these acids (5.2-13.4% cinnamein); and volatile oil (1.5-3%).
The fragrant volatile oil contains toluene, styrol, benzoic and cinnamic acids.
It also contains total balsamic acids, which is calculated on the basis of dry alcohol-soluble matter ranging between (35-50%).

cinnamein
The resins esters (30-38%) are chiefly composed of peruresinotannol cinnamate and benzoate, vanillin, free cinnamic acid and peruviol (or nerolidol).

peruviol (or nerolidol)
Uses
1. Peru balsam is a local protectant and rubefacient.
2. It also serves as a parasiticide in certain skin disorder.
3. It is used as an antiseptic and vulnerary* and is applied externally either as ointment or alone or in alcoholic solution.
4. It acts as an astringent to treat hemorrhoids.
------------------------------------------------
Vulnerary: A folk remedy or herb to promote wound healing.

3. Tolu Balsam

Synonyms Thomas balsam; Opobalsam; Resin Tolu; Balsam of Tolu.
Biological Source Tolu Balsam is a balsam obtained from Toluifera balsamum L., (Myroxylon toluiferum H.B.K.), belonging to family: Leguminosae. It is also obtained from Myroxylon balsamum (Linne') Harms. Family: Fabaceae.
Preparation Tolu Balsam is considered to be a pathological product produced in the new wood formed as a result of inflicted injury. For its preparation, it is an usual practice to make ‘V’ shaped incisions deep into the body of the main trunk. The exudate thus produced is collected either in cups or gourds held strategically just at the base of each incisions. Balsam of Tolu is collected from these cups, mixed and packed in air-tight sealed tins.
Characteristic Features It is a yellowish-brown or brown semifluid or nearly solid resinous mass. It has a characteristic aromatic vanilla-like odour and slightly pungent taste. It is usually brittle when cold. It is found to be transparent in thin layers, and shows numerous crystals of cinnamic acid. It is almost insoluble in water and petroleum ether, but freely soluble in ethanol, benzene chloroform, ether, glacial acetic acid and partially in CS2 or NaOH solution.
Chemical Constituents The drug contains resin esters (75-80%) viz., toluresinotannol cinnamate along with a small proportion of the benzoate; volatile oil (7-8%)-containing chiefly benzyl benzoate; free cinnamic acid (12-15%); free benzoic acid (2-8%); vanillin and other constituents in small quantities. It also contains cinnamein (5-13%).
Chemical Tests
1. An alcoholic solution of Tolu Balsam (0.2% w/v) where treated with a FeCl3 solution (0.5% w/v), the appearances of a green colour takes place.
2. Treatment of 1 g of the drug with 5 ml of 10% w/v KMnO4 solution when subjected to gentle heating yields benzaldehyde.
Uses
1. It is used extensively in perfumery, confectionery and chewing gums.
2. It is used widely as an expectorant in cough mixture.
3. It also finds its application as an antiseptic in the form of its tincture.

4. Benzoin

Synonyms Bitter-almond-oil camphor.
Biological Source Benzoin in the balsamic resin obtained from Styrax benzoin Dryander and Styrax paralleloneurus Perkins, generally known in trade as Sumatra Benzoin; whereas, Styrax tonkinensis (Pierre) Craib ex Hartwich, or other species of the section Anthostyrax of the genus Styrax, known commonly in the trade as Siam Benzoin both belong to the family: Styraceae.
Preparation Benzoin is also a pathological product that is obtained by incising a deep-cut in the bark. It has been observed that after a span of about eight weeks, the exudating balsamic resin tends to become less sticky in nature and firm enough to collect. The entire exudate is usually collected in two stages, namely:
Stage 1: First tapping-yields almond tears, and
Stage 2: Second tapping-yields a more fluid material.
Characteristic Features
Sumatra Benzoin: It is pertinent to mention here that in pharmacy, only the Sumatra Benzoin is used. It occurs as blocks or irregular masses of tears having variable sizes usually imbedded either in an opaque or translucent matrix. It is rather brittle, and from within the tears are milky white in appearance. It generally becomes soft when warmed and gritty when chewed. The matrix is grayish brown to reddish in colour. Its taste is quite agreeable, balsamic and resembles to that of storax. It has a resinous and aromatic taste.
Siam Benzoin: The smaller tears of Siam Benzoin are darker in colour. It occurs largely in separate concavo-convex tears which are yellowish brown to rusty brown externally, whereas milky white internally. The tears are fairly brittle but normally become soft and plastic like on being chewed. It has a vanilla-like fragrance.
Chemical Constituents The chemical constituents of the two types of Benzoin are given below:
(aSumatra Benzoin: It contains free balsamic acids, largely cinnamic acid (10%), benzoic acid (6%)-along with their corresponding ester derivatives. Besides, it also contains teriterpene acids, namely: 19-hydroxyloleanolic and 6-hydroxyoleanolic acids, cinnamyl cinnamate, phenyl propyl cinnamate, phenylethylene and lastly the traces of vanillin. It yields not less than 75% of alccohol-soluble extractives.
(bSiam Benzoin: It chiefly comprises of coniferyl benzoate (60-70%), benzoic acid (10%), triterpene siaresinol (6%) and traces of vanillin. It yields not less than 90% of alcoholsoluble extractives.

coniferyl benzoate
Chemical Tests
1. When 0.5 g of Sumatra Benzoin powder is warmed with 10 ml of KMnO4 solution (5% w/v) in a test tube, a faint and distinct odour of benzaldehyde is developed. Siam Benzoin gives a negative test.
2. When 0.2 g of Siam Benzoin powder is digested with 5 ml of ether for 5 minutes and filtered; 1 ml of the filtrate is poured into a clean china-dish containing 2-3 drops of concentrated H2SO4 and mixed carefully, a deep purplish red colouration is developed instantly. Sumatra Benzoin gives a negative test.
Uses
1. Compound benzoin tincture is frequently employed as a topical protectant.
2. It is valuable as an expectorant when vapourized.
3. It finds its usage as a cosmetic lotion usually prepared from a simple tincture.
4. Siam Benzoin has been proved to be a better preservative for lard than the Sumatra Benzoin.

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar

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0 Indian Bdellium-Synonym Scented bdellium-obtained from the bark of the naturally occurring plant Commiphora mukul Engler., Balsamodendron mukul Hook. ex. Stocks., and Commiphora weightii (Arn) Bhand

5. Indian Bdellium

Synonym Scented bdellium.
Biological Sources Indian bdellium is the oleo-gum-resin obtained from the bark of the naturally occurring plant Commiphora mukul Engler., Balsamodendron mukul Hook. ex. Stocks., and Commiphora weightii (Arn) Bhand, belonging to family: Burseraceae.
Preparation The oleo-gum-resin Indian bdellium is obtained by the incision made on the bark and the exudates are collected. Each fully grown plant produces about 0.5 to 1 kg of the product which is normally collected from January through March every year.
Characteristic Features The oleo-gum-resin from Indian bdellium has a brown to pale yellow or sometimes dull green colour. It has an agreeable balsamic and aromatic odour with a typical bitter taste. The drug is usually obtained as irregular mass, rounded or agglomerated cluster of tears. The tears are found to be transparent, having a waxy surface and quite brittle in nature. It is sticky in touch and has a fractured surface. It is partially alcohol soluble; but when triturated with water it usually gives rise to a white emulsion.
Chemical Constituents This oleo-gum-resin mostly comprises of resin (60%), gum (30%), volatile oil (1–1.5%) moisture (5%) and foreign organic substances (3-4%). The volatile oil fraction contains various terpenes, such as: β-murcene, dimyrcene, polymyrcene, caryophyllene and isocaryophyllene (Section 2.9.2).

beta-myrcene
Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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0 Myrrh-Synonyms Gum Myrrh, Myrrha-obtained from the stem and branches of Commiphora obyssinica (Berg) Engler

4. Myrrh

Synonyms Gum Myrrh, Myrrha.
Biological Source Myrrh is an oleo-gum-oresin obtained from the stem and branches of Commiphora obyssinica (Berg) Engler or from other species of Commiphora belonging to family Burseraceae.
Preparation The plants usually exude yellow coloured resin after proper incisions are made in the bark of a tree. It gradually hardens and becomes dark or reddish-brown in appearance. The mass is collected by the native tribals of Somalia for trading.
Characteristic Features Myrrh normally occurs either in the form of isolated irregular, rounded tears of 2.5 cm in diameter or as masses duly formed by the agglomeration of these tears. The tears are dull, rough and reddish-brown in appearance. It has a strong aromatic odour and possesses an acrid, bitter taste.
Chemical Constituents Myrrh contains volatile oil (7-17%), resin (20-25%), gum (57-61%), and bitter principle (3 to 4%). The volatile oil consists of eugenol, m-cresol and cuminaldehyde.
The resin is found to consist of a mixture of α-, β-, and γ-commiphoric acids (resin acids). Besides, it also contains two phenolic resins α- and β-heerabomyrrholic acids which are ether insoluble.
The oleo-gum-resin yields alcohol-soluble extract not less than 30%. It also contains phenolic compound such as: pyrocatechin and protocatechuic acid. The crude alcohol-insoluble fraction i.e., ‘gum, comprises of protein (18%) and carbohydrate (64%) made up of arabinose, galactose and glucuronic acid. However, the gum is found to be associated with an oxidase enzyme.

Protocatechuic-Acid 
Chemical Tests
1. Myrrh when triturated with water produces an yellow-emulsion.
2. When myrrh (0.1 g) is triturated with 0.5 g of pure washed sand (SiO2) in the presence of ether, filtered and evaporated on an electric water-bath, it forms a thin film of violet colour on being exposed to bromine vapours in a closed dessicator.
Uses
1. It is used chiefly in perfumes and incense.
2. It is frequently employed as an antiseptic and stimulant.
3. Myrrh acts as an astringent to the mucous membrane and hence it find its application in oral hygiene formulations, such as: gargles, mouth-washes.
4. It is also used as a carminative.

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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0 Turmeric-Synonyms Curcuma; Indian Saffron-obtained from the rhizome of Curcuma longa Linn. (Curcuma domestica Valeton)

3. Turmeric

Synonyms Curcuma; Indian Saffron; Tumeric.
Biological Source Turmeric is obtained from the rhizome of Curcuma longa Linn. (Curcuma domestica Valeton) belonging to the natural order Zingiberaceae.
Preparation The plant is normally harvested after 9-10 months when the lower leaves start becoming yellow. The rhizome is carefully dug out from the soil with a blunt knife without damaging it. The fibrous roots are discarded. The raw green turmeric is cured and processed by boiling the rhizomes with water for a duration ranging between 12-14 hours. Subsequently, the cooked rhizomes are dried in the sun for 5-7 days. Cooking process helps in achieving two objects, namely:
(a) Gelatinization of starch, and
(b) Yellow colouration, due to curcumin, spreads over the entire rhizome.
Characteristic Features Turmeric has an aromatic pepper-like but somewhat bitter taste. It gives curry dishes their characteristic yellowish colouration.
Chemical Constituents It contains volatile oil (5-6%), resin and substantial quantity of zingiberaceous starch grains. The marked and pronounced yellow colour in turmeric is due to the presence of curcuminoids which essentially contains curcumin as given below:

curcumin
The curcuma oil* obtained from turmeric contains (±)-ar-turmerone as given below:

 (±)-ar-turmerone
The volatile oil contains a host of chemical substances, such as: d-α-phellandene, d-sabinene, cineol, borneol, zingiberene, and sesquiterpenes.
Turmeric also contains some other chemical constituents, namely: p,p-dihydroxy dicinnamoylmethane; p-α-dimethy benzyl alcohol; p-hydroxy-cinnamoylferuloylmethane; 1-methyl-4-acetyl-1-cyclohexene; and caprylic acid.
Chemical Tests
1. Turmeric powder when triturated with alcohol it imparts a deep yellow colour to the resulting solution.
2. The powdered drug when treated with sulphuric acid it imparts a crimson colour.
3. The aqueous solution of turmeric with boric acid gives rise to a reddish-brown colouration which on subsequent addition of dilute alkali changes instantly to greenish-blue.
4. Turmeric powder when reacted with acetic anhydride and a few drops of concentrated sulphuric acid (36 N), it readily gives a violet colouration. Interestingly, the resulting solution when observed under the ultraviolet light (preferably in a uv-chamber), it exhibits an intense red fluorescence, which is due to the presence of Curcumin.
Uses
1. It is extensively used across the globe as a condiment as curry powder.
2. It is employed as a colouring agent for ointments.
3. It is used medicinally as a tonic, as a blood purifier, as an anthelmintic and finally as an aid to digestion.
4. It is used extennally in the form of a facial cream to improve complexion and get rid of pimples.
5. A small quantity of turmeric when boiled with milk and sugar; it helps to cure common cold and cough symptoms.
-------------------------------------------------
* H. Rupe et. al. Helv. Chim. Acta, 17, 372 (1934).

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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0 Ammoniacum-Synonym Gum ammoniac-from the flowering and fruiting stem of Dorema ammoniacum, D. Don.

2. Ammoniacum

Synonym Gum ammoniac.
Biological Source It is a oleo-gum-resin exuded from the flowering and fruiting stem of Dorema ammoniacum, D. Don. and probably other species belonging to family: Umbelliferae.
Preparation The exudation of the milky-secretions obtained in the form droplets is usually caused by the beetles that puncture the fruiting stem of D. ammoniacum. While quite a few of these milkydroplets get hardened on the stem itself, and the rest falls on the ground. The solidified oleo-gumresins are scrapped from the stem with a plant-knife and also collected from the droppings on the ground.
Characteristic Features The drug has an irregular, rounded tears, that are yellowish or browish outside and whitish from within; these are generally brittle when cold, but get softened on warming.
It is also found, in the form of mass i.e., agglomeration of small droplets. The mass is found to be darker in colour and less homogeneous.
It has a peculiar odour, slightly sweetish, bitter and somewhat acrid taste. The physical
characteristics are: mp 45-55°C and d 1.207. Its acid number varies between 60-80, whereas the saponification number ranges between 97-114. It is partly soluble in water, ethanol, ether, vineger, or alkaline solution. It readily forms an emulsion with water.
Chemical Composition Ammoniacum-the oleo-gum-resin consists of volatile oil (0.1-1.0%), resin (65-70%), gum (20%), moisture (2-12%), insoluble residue (3.5%) and ash (1%). Ammoresinol, a phenolic substance is the main constituent of the resin, which is a colourless crystal, mp 110°C. It also contains traces of salicylic acid.
Chemical Tests
1. Ammoniacum when triturated with water, it forms a white emulsion.
2. A portion of the above emulsion when treated with a solution of chlorinated soda gives a deep orange-red colouration.
3. A portion of the emulsion on being treated with a potash solution yields a yellow colour.
4. A portion of the emulsion when treated with a 0.1% (w/v) solution of FeCl3, it gives an instant violet colouration due to the presence of traces of salicylic acid.
Uses
1. It is an important ingredient of porcelain cements.
2. It is a stimulant, and secreted by the bronchial mucous surface, thereby disinfecting the secretions.
3. It is used in plaster-of-paris (POP) plasters as a stimulant to the skin.
4. It is also used as a disinfectant expectorant in chronic bronchitis amalgamated with excessive discharge.

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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0 Asafoetida-Synonyms Asafetida; Asant; Devil's dung; Food of the Gods; Gum Asafoetida

1. Asafoetida

Synonyms Asafetida; Asant; Devil's dung; Food of the Gods; Gum Asafoetida.
Biological Sources Asafoetida the oleo-gum-resin is obtained as an exudation of the decapitated rhizome on roots of Ferula assafoetida L.; Ferula foetida Regel, and some other species of Ferula, belonging to the nature order Umbelliferae.
Preparation Asafoetida is generally present as a milky liquid in the large schizogenous ducts and lysigenous cavities. However, these ducts and cavities are located more intensively in the cortex region of the stem and root. The drug is obtaining chiefly from the stem.
The fully grown plants are usually cut down to the crown region during the spring. The exposed surface is protected by a dome-like covering made up of twigs and leaves. After about a month, the hardened resinous substance is collected by scrapping. Likewise, the stems are also cut off and thereby additional collections of asafoetida are made frequently at an interval of 10 days unless and until the exudation ceases to ooze. Furthermore, it is also collected from the root by exposing its crown and excising the stem. The oleo-gum-resin exudes from the cut surface of the root and the former is collected soonafter it gets dried. Thus, the entire collection of asafoetida from the various portions of the plant are mixed together and dried in the sun.
Characteristic Features The drug occurs normally as soft mass or irregular lumps or ‘tears’ or agglomeration of tears. The tears are brittle and tough. Asafoetida has a strong, alliaceous, persistent garlic-like odour and having a bitter acrid taste. This oleo-gum-resin when triturated with water it gives a milky emulsion.
Chemical Constituents Asafoetida contains volatile oil (8-16°C) gum (25%) and resin (40-60%).
The volatile oil essentially consists of some organic sulphides solely responsible for attributing the characteristic garlic-like odour. The resin cousists of notannol, asaresinotannol i.e., the resin alcohols, which are present partially in the free state and partially in the combined form with ferulic acid. It also contains umbellic acid and umbelliferone; the latter is found combined with ferulic acid, but it gets generated on being treated with dilute HCl.

umbelliferone
There are three sulphur-compounds that have been isolated from the asafoctida resin, namely:
(a) 1-Methylpropyl-1-propenyl disulphide,
(b) 1-(Methylthio) propyl-1-propenyl disulphide, and
(c) 1-Methylpropyl-3-(methylthio)-2- propenyl disulphide.
Interestingly, the latter two (i.e., ‘b’ and ‘c’) have pesticidal properties.
Chemical Tests
1. It forms an instant milky-white emulsion when triturated with water owing to the presence of gum.
2. The freshly fractured surface when treated with a drop of sulphuric acid (conc.), it gives rise to a reddish-brown colour which on being washed with water changes to violet colouration.
3. Likewise, when the freshly fractured surface is treated with nitric acid (50%), it produces a green colour readily.
4. Boil 1 g asafoetida powder with HCl (50%), filter and make the filtrate strongly alkaline with NH4OH (conc.), it gives a blue fluorescence. It is also known as the Umbelliferone Test.
Uses
1. It is abundantly used in India and Iran as a common condiment and flavouring agent in food products.
2. It is also an important ingredient in Worcestershire Sauce.
3. It is used as a repellant [2% (w/v) suspension] against dogs, cats, deer, rabbits etc.
4. It is used seldomly as an antispasmodic, carminative, expedorant and laxative.
5. It is still employed in veterinary externally to prevent bandage chewing by dogs.
6. It is also used as a powerful nerving stimulant especially in nervous disorders related to hysteria.

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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0 Oleo-Gum-Resins

2.9 Oleo-Gum-Resins

The oleo-gum-resins are the naturally occurring mixture of resin, gum, volatile oil, and mostly small quantities of other substances.
There are some potent oleo-gum-resins which exhibit remarkable medicinal values. A few such drugs shall be discussed briefly here under: Asafoetida; Ammoniacum; Turmeric; Myrrh; Indian Bdellium etc.

1. Asafoetida

Synonyms Asafetida; Asant; Devil's dung; Food of the Gods; Gum Asafoetida.
Biological Sources Asafoetida the oleo-gum-resin is obtained as an exudation of the decapitated rhizome on roots of Ferula assafoetida L.; Ferula foetida Regel, and some other species of Ferula, belonging to the nature order Umbelliferae.
Preparation Asafoetida is generally present as a milky liquid in the large schizogenous ducts and lysigenous cavities. However, these ducts and cavities are located more intensively in the cortex region of the stem and root. The drug is obtaining chiefly from the stem.
The fully grown plants are usually cut down to the crown region during the spring. The exposed surface is protected by a dome-like covering made up of twigs and leaves. After about a month, the hardened resinous substance is collected by scrapping. Likewise, the stems are also cut off and thereby additional collections of asafoetida are made frequently at an interval of 10 days unless and until the exudation ceases to ooze. Furthermore, it is also collected from the root by exposing its crown and excising the stem. The oleo-gum-resin exudes from the cut surface of the root and the former is collected soonafter it gets dried. Thus, the entire collection of asafoetida from the various portions of the plant are mixed together and dried in the sun.
Characteristic Features The drug occurs normally as soft mass or irregular lumps or ‘tears’ or agglomeration of tears. The tears are brittle and tough. Asafoetida has a strong, alliaceous, persistent garlic-like odour and having a bitter acrid taste. This oleo-gum-resin when triturated with water it gives a milky emulsion.
Chemical Constituents Asafoetida contains volatile oil (8-16°C) gum (25%) and resin (40-60%).
The volatile oil essentially consists of some organic sulphides solely responsible for attributing the characteristic garlic-like odour. The resin cousists of notannol, asaresinotannol i.e., the resin alcohols, which are present partially in the free state and partially in the combined form with ferulic acid. It also contains umbellic acid and umbelliferone; the latter is found combined with ferulic acid, but it gets generated on being treated with dilute HCl.

umbelliferone
There are three sulphur-compounds that have been isolated from the asafoctida resin, namely:
(a) 1-Methylpropyl-1-propenyl disulphide,
(b) 1-(Methylthio) propyl-1-propenyl disulphide, and
(c) 1-Methylpropyl-3-(methylthio)-2- propenyl disulphide.
Interestingly, the latter two (i.e., ‘b’ and ‘c’) have pesticidal properties.
Chemical Tests
1. It forms an instant milky-white emulsion when triturated with water owing to the presence of gum.
2. The freshly fractured surface when treated with a drop of sulphuric acid (conc.), it gives rise to a reddish-brown colour which on being washed with water changes to violet colouration.
3. Likewise, when the freshly fractured surface is treated with nitric acid (50%), it produces a green colour readily.
4. Boil 1 g asafoetida powder with HCl (50%), filter and make the filtrate strongly alkaline with NH4OH (conc.), it gives a blue fluorescence. It is also known as the Umbelliferone Test.
Uses
1. It is abundantly used in India and Iran as a common condiment and flavouring agent in food products.
2. It is also an important ingredient in Worcestershire Sauce.
3. It is used as a repellant [2% (w/v) suspension] against dogs, cats, deer, rabbits etc.
4. It is used seldomly as an antispasmodic, carminative, expedorant and laxative.
5. It is still employed in veterinary externally to prevent bandage chewing by dogs.
6. It is also used as a powerful nerving stimulant especially in nervous disorders related to hysteria.

2. Ammoniacum

Synonym Gum ammoniac.
Biological Source It is a oleo-gum-resin exuded from the flowering and fruiting stem of Dorema ammoniacum, D. Don. and probably other species belonging to family: Umbelliferae.
Preparation The exudation of the milky-secretions obtained in the form droplets is usually caused by the beetles that puncture the fruiting stem of D. ammoniacum. While quite a few of these milkydroplets get hardened on the stem itself, and the rest falls on the ground. The solidified oleo-gumresins are scrapped from the stem with a plant-knife and also collected from the droppings on the ground.
Characteristic Features The drug has an irregular, rounded tears, that are yellowish or browish outside and whitish from within; these are generally brittle when cold, but get softened on warming.
It is also found, in the form of mass i.e., agglomeration of small droplets. The mass is found to be darker in colour and less homogeneous.
It has a peculiar odour, slightly sweetish, bitter and somewhat acrid taste. The physical
characteristics are: mp 45-55°C and d 1.207. Its acid number varies between 60-80, whereas the saponification number ranges between 97-114. It is partly soluble in water, ethanol, ether, vineger, or alkaline solution. It readily forms an emulsion with water.
Chemical Composition Ammoniacum-the oleo-gum-resin consists of volatile oil (0.1-1.0%), resin (65-70%), gum (20%), moisture (2-12%), insoluble residue (3.5%) and ash (1%). Ammoresinol, a phenolic substance is the main constituent of the resin, which is a colourless crystal, mp 110°C. It also contains traces of salicylic acid.
Chemical Tests
1. Ammoniacum when triturated with water, it forms a white emulsion.
2. A portion of the above emulsion when treated with a solution of chlorinated soda gives a deep orange-red colouration.
3. A portion of the emulsion on being treated with a potash solution yields a yellow colour.
4. A portion of the emulsion when treated with a 0.1% (w/v) solution of FeCl3, it gives an instant violet colouration due to the presence of traces of salicylic acid.
Uses
1. It is an important ingredient of porcelain cements.
2. It is a stimulant, and secreted by the bronchial mucous surface, thereby disinfecting the secretions.
3. It is used in plaster-of-paris (POP) plasters as a stimulant to the skin.
4. It is also used as a disinfectant expectorant in chronic bronchitis amalgamated with excessive discharge.

3. Turmeric

Synonyms Curcuma; Indian Saffron; Tumeric.
Biological Source Turmeric is obtained from the rhizome of Curcuma longa Linn. (Curcuma domestica Valeton) belonging to the natural order Zingiberaceae.
Preparation The plant is normally harvested after 9-10 months when the lower leaves start becoming yellow. The rhizome is carefully dug out from the soil with a blunt knife without damaging it. The fibrous roots are discarded. The raw green turmeric is cured and processed by boiling the rhizomes with water for a duration ranging between 12-14 hours. Subsequently, the cooked rhizomes are dried in the sun for 5-7 days. Cooking process helps in achieving two objects, namely:
(a) Gelatinization of starch, and
(b) Yellow colouration, due to curcumin, spreads over the entire rhizome.
Characteristic Features Turmeric has an aromatic pepper-like but somewhat bitter taste. It gives curry dishes their characteristic yellowish colouration.
Chemical Constituents It contains volatile oil (5-6%), resin and substantial quantity of zingiberaceous starch grains. The marked and pronounced yellow colour in turmeric is due to the presence of curcuminoids which essentially contains curcumin as given below:

curcumin
The curcuma oil* obtained from turmeric contains (±)-ar-turmerone as given below:

 (±)-ar-turmerone
The volatile oil contains a host of chemical substances, such as: d-α-phellandene, d-sabinene, cineol, borneol, zingiberene, and sesquiterpenes.
Turmeric also contains some other chemical constituents, namely: p,p-dihydroxy dicinnamoylmethane; p-α-dimethy benzyl alcohol; p-hydroxy-cinnamoylferuloylmethane; 1-methyl-4-acetyl-1-cyclohexene; and caprylic acid.
Chemical Tests
1. Turmeric powder when triturated with alcohol it imparts a deep yellow colour to the resulting solution.
2. The powdered drug when treated with sulphuric acid it imparts a crimson colour.
3. The aqueous solution of turmeric with boric acid gives rise to a reddish-brown colouration which on subsequent addition of dilute alkali changes instantly to greenish-blue.
4. Turmeric powder when reacted with acetic anhydride and a few drops of concentrated sulphuric acid (36 N), it readily gives a violet colouration. Interestingly, the resulting solution when observed under the ultraviolet light (preferably in a uv-chamber), it exhibits an intense red fluorescence, which is due to the presence of Curcumin.
Uses
1. It is extensively used across the globe as a condiment as curry powder.
2. It is employed as a colouring agent for ointments.
3. It is used medicinally as a tonic, as a blood purifier, as an anthelmintic and finally as an aid to digestion.
4. It is used extennally in the form of a facial cream to improve complexion and get rid of pimples.
5. A small quantity of turmeric when boiled with milk and sugar; it helps to cure common cold and cough symptoms.
-------------------------------------------------
* H. Rupe et. al. Helv. Chim. Acta17, 372 (1934).

4. Myrrh

Synonyms Gum Myrrh, Myrrha.
Biological Source Myrrh is an oleo-gum-oresin obtained from the stem and branches of Commiphora obyssinica (Berg) Engler or from other species of Commiphora belonging to family Burseraceae.
Preparation The plants usually exude yellow coloured resin after proper incisions are made in the bark of a tree. It gradually hardens and becomes dark or reddish-brown in appearance. The mass is collected by the native tribals of Somalia for trading.
Characteristic Features Myrrh normally occurs either in the form of isolated irregular, rounded tears of 2.5 cm in diameter or as masses duly formed by the agglomeration of these tears. The tears are dull, rough and reddish-brown in appearance. It has a strong aromatic odour and possesses an acrid, bitter taste.
Chemical Constituents Myrrh contains volatile oil (7-17%), resin (20-25%), gum (57-61%), and bitter principle (3 to 4%). The volatile oil consists of eugenol, m-cresol and cuminaldehyde.
The resin is found to consist of a mixture of α-, β-, and γ-commiphoric acids (resin acids). Besides, it also contains two phenolic resins α- and β-heerabomyrrholic acids which are ether insoluble.
The oleo-gum-resin yields alcohol-soluble extract not less than 30%. It also contains phenolic compound such as: pyrocatechin and protocatechuic acid. The crude alcohol-insoluble fraction i.e., ‘gum, comprises of protein (18%) and carbohydrate (64%) made up of arabinose, galactose and glucuronic acid. However, the gum is found to be associated with an oxidase enzyme.

Protocatechuic-Acid 
Chemical Tests
1. Myrrh when triturated with water produces an yellow-emulsion.
2. When myrrh (0.1 g) is triturated with 0.5 g of pure washed sand (SiO2) in the presence of ether, filtered and evaporated on an electric water-bath, it forms a thin film of violet colour on being exposed to bromine vapours in a closed dessicator.
Uses
1. It is used chiefly in perfumes and incense.
2. It is frequently employed as an antiseptic and stimulant.
3. Myrrh acts as an astringent to the mucous membrane and hence it find its application in oral hygiene formulations, such as: gargles, mouth-washes.
4. It is also used as a carminative.

5. Indian Bdellium

Synonym Scented bdellium.
Biological Sources Indian bdellium is the oleo-gum-resin obtained from the bark of the naturally occurring plant Commiphora mukul Engler., Balsamodendron mukul Hook. ex. Stocks., and Commiphora weightii (Arn) Bhand, belonging to family: Burseraceae.
Preparation The oleo-gum-resin Indian bdellium is obtained by the incision made on the bark and the exudates are collected. Each fully grown plant produces about 0.5 to 1 kg of the product which is normally collected from January through March every year.
Characteristic Features The oleo-gum-resin from Indian bdellium has a brown to pale yellow or sometimes dull green colour. It has an agreeable balsamic and aromatic odour with a typical bitter taste. The drug is usually obtained as irregular mass, rounded or agglomerated cluster of tears. The tears are found to be transparent, having a waxy surface and quite brittle in nature. It is sticky in touch and has a fractured surface. It is partially alcohol soluble; but when triturated with water it usually gives rise to a white emulsion.
Chemical Constituents This oleo-gum-resin mostly comprises of resin (60%), gum (30%), volatile oil (1–1.5%) moisture (5%) and foreign organic substances (3-4%). The volatile oil fraction contains various terpenes, such as: β-murcene, dimyrcene, polymyrcene, caryophyllene and isocaryophyllene (Section 2.9.2).

beta-myrcene

Source:Pharmacognosy And Pharmacobiotechnology By Ashutosh Kar
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