![]() Dihydrocapsaicin structure
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Common Name | Dihydrocapsaicin | ||
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CAS Number | 19408-84-5 | Molecular Weight | 307.428 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 457.3±55.0 °C at 760 mmHg | |
Molecular Formula | C18H29NO3 | Melting Point | 62-65 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 230.4±31.5 °C | |
Symbol |
![]() GHS06 |
Signal Word | Danger |
Use of DihydrocapsaicinDihydrocapsaicin is a natural capsaicin, acts as a selective TRPV1 agonist, and also increases p-Akt levels. Dihydrocapsaicin enhances the hypothermia-induced neuroprotection[1][2]. |
Name | dihydrocapsaicin |
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Synonym | More Synonyms |
Description | Dihydrocapsaicin is a natural capsaicin, acts as a selective TRPV1 agonist, and also increases p-Akt levels. Dihydrocapsaicin enhances the hypothermia-induced neuroprotection[1][2]. |
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Related Catalog | |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 457.3±55.0 °C at 760 mmHg |
Melting Point | 62-65 °C(lit.) |
Molecular Formula | C18H29NO3 |
Molecular Weight | 307.428 |
Flash Point | 230.4±31.5 °C |
Exact Mass | 307.214752 |
PSA | 58.56000 |
LogP | 4.72 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.508 |
Storage condition | 2-8°C |
Water Solubility | H2O: insoluble |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATAMUTATION DATA
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Symbol |
![]() GHS06 |
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Signal Word | Danger |
Hazard Statements | H301-H315-H319-H335 |
Precautionary Statements | P261-P301 + P310-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges |
Hazard Codes | T:Toxic; |
Risk Phrases | R25;R36/37/38 |
Safety Phrases | S22-S26-S28-S36/39-S45-S36/37/39 |
RIDADR | UN 2811 6.1/PG 2 |
WGK Germany | 3 |
RTECS | RA8530000 |
Packaging Group | II |
Hazard Class | 6.1(a) |
HS Code | 3302109090 |
Precursor 9 | |
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DownStream 0 |
HS Code | 2924299090 |
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Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Chemical genetics reveals a complex functional ground state of neural stem cells.
Nat. Chem. Biol. 3(5) , 268-273, (2007) The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain canc... |
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Inhibition by capsaicin and its related vanilloids of compound action potentials in frog sciatic nerves.
Life Sci. 92(6-7) , 368-78, (2013) Although capsaicin not only activates transient receptor potential vanilloid-1 (TRPV1) channels but also inhibits nerve conduction, the latter action has not yet been fully examined. The purpose of th... |
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Optimization and validation of liquid chromatography and headspace-gas chromatography based methods for the quantitative determination of capsaicinoids, salicylic acid, glycol monosalicylate, methyl salicylate, ethyl salicylate, camphor and l-menthol in a topical formulation.
J. Pharm. Biomed. Anal. 60 , 51-8, (2012) Capsaicinoids, salicylic acid, methyl and ethyl salicylate, glycol monosalicylate, camphor and l-menthol are widely used in topical formulations to relieve local pain. For each separate compound or si... |
N-(4-Hydroxy-3-methoxybenzyl)-8-methylnonanamide |
Nonanimidic acid, N-[(4-hydroxy-3-methoxyphenyl)methyl]-8-methyl-, (1Z)- |
(1Z)-N-(4-Hydroxy-3-methoxybenzyl)-8-methylnonanimidic acid |
6,7-Dihydrocapsaicin |
8-methyl-nonanoic acid vanillylamide |
N-[(4-Hydroxy-3-methoxy-phenyl)methyl]-8-methyl-nonanamide |
Nonanamide,8-methyl-N-vanillyl |
Dihydro Capsaicin |
MFCD00017259 |
N-[(4-hydroxy-3-methoxyphenyl)methyl]-8-methylnonanamide |
Nonanamide, N-[(4-hydroxy-3-methoxyphenyl)methyl]-8-methyl- |
8-Methyl-N-vanillyl-nonamide |
Dihydrocapsaicin |
Nonanamide, 8-methyl-N-vanillyl- |
EINECS 206-969-8 |
8-Methyl-N-vanillylnonanamide |
N-(4-hydroxy-3-methoxybenzyl)isodecanamide |