1945
DOI: 10.1126/science.102.2646.279
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The Relation of Hypersensitiveness to Poison Ivy and to Cashew Nut Shell Liquid

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Cited by 20 publications
(27 citation statements)
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“…CNSL can be regarded as a versatile and valuable raw material for polymer production and represents a good natural alternative to petrochemicals derived phenols [10]. CNSL constitutes nearly 25% of the total weight of the nut and is composed of anacardic acid (3-n-pentadecylsalicylic acid) and smaller amounts of cardanol (3-n-pentadecylphenol), cardol (5-npentadecylresorcinol), and methylcardol (2-methyl-5-n-pentadecylresorcinol), the long aliphatic side-chain being saturated, mono-olefinic (8), di-olefinic (8,11), and triolefinic (8,11,14) with an average value of two double bonds per molecule ( Fig. 1).…”
Section: Introductionmentioning
confidence: 99%
“…CNSL can be regarded as a versatile and valuable raw material for polymer production and represents a good natural alternative to petrochemicals derived phenols [10]. CNSL constitutes nearly 25% of the total weight of the nut and is composed of anacardic acid (3-n-pentadecylsalicylic acid) and smaller amounts of cardanol (3-n-pentadecylphenol), cardol (5-npentadecylresorcinol), and methylcardol (2-methyl-5-n-pentadecylresorcinol), the long aliphatic side-chain being saturated, mono-olefinic (8), di-olefinic (8,11), and triolefinic (8,11,14) with an average value of two double bonds per molecule ( Fig. 1).…”
Section: Introductionmentioning
confidence: 99%
“…The irritant and allergenic potency ranges in descending order from cardol to anacardic acid and anacardols (Keil et al 1945a;Wasserman and Dawson 1948). All have 15 carbon monoene or diene side chains, which, as is typical of the family, are closely related chemically and allergenically to the catechol -derived urushiols in Toxicodendron (poison ivy) (Keil et al 1945b;Mitchell and Rook 1979). All have 15 carbon monoene or diene side chains, which, as is typical of the family, are closely related chemically and allergenically to the catechol -derived urushiols in Toxicodendron (poison ivy) (Keil et al 1945b;Mitchell and Rook 1979).…”
Section: Anacardium Lmentioning
confidence: 99%
“…All have 15 carbon monoene or diene side chains, which, as is typical of the family, are closely related chemically and allergenically to the catechol -derived urushiols in Toxicodendron (poison ivy) (Keil et al 1945b;Mitchell and Rook 1979). Species of Anacardium, Schinus, and Toxicodendron share similar toxicants, and there is considerable allergic cross -reactivity among them (Keil et al 1945a;ElSohly et al 1986). These derivatives are referred to as cardanol 15:0, 15:1, and 15:2, based upon the number of side chain carbons and double bonds.…”
Section: Anacardium Lmentioning
confidence: 99%
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“…Discussion The occurence of a Rhus poisonous tree in Central and nor thern South America (2), deserves medical attention. This tree may cause dermatitis venenata and induce cross sensitization to other Anacardiaceae, a common trend in members of this family (4,5).…”
mentioning
confidence: 99%