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Key Documents

360376

Sigma-Aldrich

Capsaicin

63.7% (HPLC), powder, TRPV1 agonist

Synonyme(s) :

8-Methyl-N-vanillyl-trans-6-nonenamide

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About This Item

Formule linéaire :
(CH3)2CHCH=CH(CH2)4CONHCH2C6H3-4-(OH)-3-(OCH3)
Numéro CAS:
Poids moléculaire :
305.41
Numéro Beilstein :
2816484
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352200
ID de substance PubChem :
Nomenclature NACRES :
NA.77

product name

Capsaicin, natural

Qualité

natural

Pureté

63.7% (HPLC)

Forme

powder

Composition

capsaicin, 65%
dihydrocapsaicin, 35%

Pf

62-65 °C (lit.)

Solubilité

chloroform: 5%

Température de stockage

2-8°C

Chaîne SMILES 

COc1cc(CNC(=O)CCCC\C=C\C(C)C)ccc1O

InChI

1S/C18H27NO3/c1-14(2)8-6-4-5-7-9-18(21)19-13-15-10-11-16(20)17(12-15)22-3/h6,8,10-12,14,20H,4-5,7,9,13H2,1-3H3,(H,19,21)/b8-6+

Clé InChI

YKPUWZUDDOIDPM-SOFGYWHQSA-N

Informations sur le gène

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Description générale

Capsaicin (Zostrix), an alkaloid extract is obtained from hot chili peppers. It is accessible in the form of cream and lotion. Capsaicin is a hydrophobic, instable and pungent white crystalline powder, that has no smell and color. It is produced by mixing a branched-chain fatty acid to vanillylamine in the chili pepper.

Application

Capsaicin has been used in the development of the isolation methods. It has also been used in the development of enzyme based electrochemical biosensor for the determination of capsaicin using a novel signal amplification strategy.

Actions biochimiques/physiologiques

Capsaicin is used as an important component of oleoresin capsicum or pepper spray. It plays a beneficial role in obesity, cardiovascular and gastrointestinal conditions, several cancers, neurogenic bladder and dermatologic conditions. It is used in the production of spices, chilli sauces and pain-inducing defensive pepper sprays. Capsaicin is also used to manufacture creams to treat diabetic neuropathy, cluster headache, psoriasis, rheumatoid arthritis and reflex sympathetic dystrophy. It is considered as an agonist of the transient receptor potential cation channel subfamily V member 1 (TrpV1).
Prototype vanilloid receptor agonist. Neurotoxin; activates sensory neurons that give rise to unmyelinated C-fibers, many of which contain substance P. Topical application desensitizes the sensory nerve endings giving a paradoxical antinociceptive effect; systemic administration can be neurotoxic to capsaicin-sensitive cells, especially in newborn animals. Active component of chili peppers.

Pictogrammes

Skull and crossbonesHealth hazardCorrosion

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 2 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

235.4 °F - closed cup

Point d'éclair (°C)

113 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


Certificats d'analyse (COA)

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Les clients ont également consulté

Postherpetic neuralgia
Christo P J and Cauley B D
Headache, 48, 130-134 (2008)
Mechanisms and clinical uses of capsaicin
Sharma S K, et al.
European Journal of Pharmacology, 720(1-3), 55-62 (2013)
Isolation of individual capsaicinoids from a mixture and their characterization by 13C NMR spectrometry
Thompson R Q, et al.
Talanta, 70(2), 315-322 (2006)
Electrochemical sensing platform amplified with a nanobiocomposite of L-phenylalanine ammonia-lyase enzyme for the detection of capsaicin
Sabela M I, et al.
Biosensors And Bioelectronics, 45-53 (2016)
Capsaicin, the primary constituent of pepper sprays and its pharmacological effects on mammalian ocular tissues
Krishnatreyya H, et al.
European Journal of Pharmacology, 819, 114-121 (2018)

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