Tolu balsam

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Balsam of Tolu Balsamum tolutanum1.JPG
Balsam of Tolu

Tolu balsam [1] or balsam of Tolu [2] is a balsam that originates from South America (Colombia, Peru, Venezuela). It is similar to (and frequently confounded with) the balsam of Peru.

Contents

It is tapped from the living trunks of Myroxylon balsamum var. balsamum. [1] The fresh balsam of Tolu is a brownish, sticky, semifluid mass. It gradually becomes a brittle solid, but softens again when it is warm. [2] The balsam contains a fairly large amount of benzyl benzoate and benzyl cinnamate. [3]

Collection

Balsam of Tolu is obtained by cutting a V-shaped wound on the trunk of Myroxylon balsamum var. balsamum and fixing a calabash there to catch the exuded resin. [2]

Uses

The resin is still used in certain cough syrup formulas. However its main use in the modern era is in perfumery, where it is valued for its warm, mellow yet somewhat spicy scent.

It is also used as a natural remedy for skin rashes. It is a well known cause of contact dermatitis, a form of skin allergy.

History

In 1841, Henri Étienne Sainte-Claire Deville isolated toluene by the dry distillation of tolu balsam. [4] The resin is used in traditional medicine by the people of Central America and South America. [5] It got its name because it was shipped to Europe from Tolú, Colombia. [2] In 1753 Linnaeus described the type specimen of Toluifera balsamum (the synonym of Myroxylon balsamum) using a specimen collected in the province of Cartagena, probably a town called Tolú, which at the time was located in the province of Cartagena, and named it Toluifera balsamum in relation to the place of collection. [6] The name of the important hydrocarbon solvent toluene is derived from Tolu balsam.

Related Research Articles

<span class="mw-page-title-main">Toluene</span> Chemical compound

Toluene, also known as toluol, is a substituted aromatic hydrocarbon with the chemical formula C6H5CH3, often abbreviated as PhCH3, where Ph stands for the phenyl group. It is a colorless, water-insoluble liquid with the odor associated with paint thinners. It is a mono-substituted benzene derivative, consisting of a methyl group (CH3) attached to a phenyl group by a single bond. As such, its systematic IUPAC name is methylbenzene. Toluene is predominantly used as an industrial feedstock and a solvent.

<span class="mw-page-title-main">Resin</span> Organic polymer, typically from plants

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<span class="mw-page-title-main">Benzoin (resin)</span> Balsamic resin from trees in genus Styrax

Benzoin or benjamin is a balsamic resin obtained from the bark of several species of trees in the genus Styrax. It is used in perfumes and some kinds of incense and as a flavoring and medicine. It is distinct from the chemical compound benzoin, which is ultimately derived chemically from benzoin resin; the primary active ingredient of benzoin resin is actually benzoic acid, not benzoin.

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<span class="mw-page-title-main">Storax balsam</span> Resin from the genus liquidambar

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<i>Myroxylon</i> Genus of legumes

Myroxylon is a genus of Fabaceae native to Latin America.

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Benzyl benzoate is an organic compound which is used as a medication and insect repellent. As a medication it is used to treat scabies and lice. For scabies either permethrin or malathion is typically preferred. It is applied to the skin as a lotion. Typically two to three applications are needed. It is also present in Balsam of Peru, Tolu balsam, and in a number of flowers.

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<span class="mw-page-title-main">Balsam of Peru</span> Type of tree balsam

Balsam of Peru or Peru balsam, also known and marketed by many other names, is a balsam derived from a tree known as Myroxylon balsamum var. pereirae; it is found in El Salvador, where it is an endemic species.

<span class="mw-page-title-main">Stacte</span> Unknown biblical substance used in incense

Stacte and nataph are names used for one component of the Solomon's Temple incense, the Ketoret, specified in the Book of Exodus. Variously translated to the Greek term or to an unspecified "gum resin" or similar, it was to be mixed in equal parts with onycha, galbanum and mixed with pure frankincense and they were to "beat some of it very small" for burning on the altar of the tabernacle.

In organic chemistry, transalkylation is a chemical reaction involving the transfer of an alkyl group from one organic compound to another. The reaction is used for the transfer of methyl and ethyl groups between benzene rings. This is of particular value in the petrochemical industry to manufacture p-xylene, styrene, and other aromatic compounds. Motivation for using transalkylation reactions is based on a difference in production and demand for benzene, toluene, and xylenes. Transalkylation can convert toluene, which is overproduced, into benzene and xylene, which are under-produced. Zeolites are often used as catalysts in transalkylation reactions.

<span class="mw-page-title-main">Opopanax (perfumery)</span>

Opopanax is the commercial name of bisabol or bissabol, the fragrant oleo-gum-resin of Commiphora guidottii. It has been a major export article from Somalia since ancient times, and is called hebbakhade, habaghadi or habak hadi in Somali. It is an important ingredient in perfumery and therefore known as scented myrrh, sweet myrrh, perfumed myrrh or perfumed bdellium.

Resinoids are extracts of resinous plant exudates.

<i>Myroxylon balsamum</i> Species of legume

Myroxylon balsamum, Santos mahogany, is a species of tree in the family Fabaceae. It is native to tropical forests from Southern Mexico through the Amazon regions of Peru and Brazil at elevations of 200–690 metres (660–2,260 ft). Plants are found growing in well drained soil in evergreen humid forest.

References

  1. 1 2 "Assessment report on Myroxylon balsamum (L.) Harms var. pereirae (Royle) Harms, balsamum" (PDF). European Medicines Agency. Committee on Herbal Medicinal Products (HMPC). 2016-05-31. Retrieved 2021-03-09.
  2. 1 2 3 4 Flückiger, Friedrich August; Hanbury, Daniel (1874). Pharmacographia: A History of the Principal Drugs of Vegetable Origin, Met with in Great Britain and British India. London: Macmillan and Co. pp. 177–184.
  3. Karl-Georg Fahlbusch; et al. (2007), "Flavors and Fragrances", Ullmann's Encyclopedia of Industrial Chemistry (7th ed.), Wiley, p. 116
  4. Jörg Fabri; et al. (2007), "Toluene", Ullmann's Encyclopedia of Industrial Chemistry (7th ed.), Wiley, p. 4
  5. James A. Duke (2009), "Tolu Balsam Tree", Duke's Handbook of Medicinal Plants of Latin America, CRC Press, pp. 474–475
  6. Bagnatori Sartori, Ângela Lúcia; Lewis, Gwilym P.; Mansano, Vidal de Freitas; Tozzi, Ana Maria Goulart de Azevedo (6 November 2015). "A revision of the genus Myroxylon (Leguminosae: Papilionoideae)". Kew Bulletin. 70 (4): 48. Bibcode:2015KewBu..70...48S. doi:10.1007/s12225-015-9604-7. S2CID   26434950.