| Weight | 153.181 g/mol |
|---|---|
| Formula | C8H11NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Vanillylamine (1196-92-5)
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- Sigma-Aldrich - Vanillylamine200.00 USD
- Fisher Scientific - Search for Vanillylamine
- TCI - Search for Vanillylamine
- Biotransformation of ferulic acid and vanillylamine to capsaicin and vanillin in immobilized cell cultures of Capsicum frutescens (Plant Cell Tissue and Organ Culture, 1996)
- Encapsulation of vanillylamine by native and modified cyclodextrins: Spectral and computational studies (Journal of Molecular Structure, 2012)
- Lipase-catalyzed synthesis of capsaicin analogs by amidation of vanillylamine with fatty acid derivatives (Biotechnology Letters, 1998)
- Vanillin formation by microbial amine oxidases from vanillylamine (Journal of Fermentation and Bioengineering, 1997)
- Utilization of capsaicin and vanillylamine as growth substrates by Capsicum (hot pepper)associated bacteria (Environmental Microbiology, 2006)
- Enzymatic hydrolysis of capsaicins for the production of vanillylamine using ECB deacylase from Actinoplanes utahensis (Food Chemistry, 2011)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=C(C=CC(=C1)CN)O
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InChIKeyWRPWWVNUCXQDQV-UHFFFAOYSA-N
- Pubchem - Vanillylamine
- Wikipedia - vanillylamine
Vanillylamine is an alkaloid that is an intermediate in the biosynthesis of capsaicin. Vanillylamine is produced from vanillin by the enzyme vanillin aminotransferase. It is then converted with 8-methyl-6-nonenoic acid into capsaicin by the enzyme capsaicin synthase.
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Vanillylamine
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