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94752

Sigma-Aldrich

Vanilline

tested according to Ph. Eur.

Synonyme(s) :

4-hydroxy-3-méthoxybenzaldéhyde, Aldéhyde vanillique

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About This Item

Formule linéaire :
4-(HO)C6H3-3-(OCH3)CHO
Numéro CAS:
121-33-5
Poids moléculaire :
152.15
Numéro Beilstein :
472792
Numéro CE :
204-465-2
Numéro MDL:
MFCD00006942
Code UNSPSC :
41116107
ID de substance PubChem :
329770383
Nomenclature NACRES :
NA.21

Agence

USP/NF
tested according to Ph. Eur.

Niveau de qualité

200

Densité de vapeur

5.3 (vs air)

Pression de vapeur

>0.01 mmHg ( 25 °C)

Pureté

99.0-101.0% dry basis

Forme

powder or crystals

Point d'ébullition

170 °C/15 mmHg (lit.)

Pf

81-83 °C (lit.)

Solubilité

water: slightly soluble 10 g/L at 25 °C

Application(s)

hematology
histology
pharmaceutical (small molecule)

Température de stockage

room temp

Chaîne SMILES 

COc1cc(C=O)ccc1O

InChI

1S/C8H8O3/c1-11-8-4-6(5-9)2-3-7(8)10/h2-5,10H,1H3

Clé InChI

MWOOGOJBHIARFG-UHFFFAOYSA-N

Informations sur le gène

rat ... Ar(24208)

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Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H319

Classification des risques

Eye Irrit. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

319.6 - 321.4 °F - closed cup

Point d'éclair (°C)

159.8 - 160.8 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
BCCM0820
BCCL5001
BCCL1553
BCCJ3673
BCCH2819

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Igor A O Reis et al.
Food chemistry, 135(4), 2453-2461 (2012-09-18)
A single-step selective separation of two food additives was investigated using alcohol-salt aqueous two-phase systems (ATPS). The selective partitioning of two of the most used additives from a processed food waste material, vanillin and l-ascorbic acid, was successfully accomplished. The
Yavuz Yardım et al.
Food chemistry, 141(3), 1821-1827 (2013-07-23)
A method for the determination of food additive vanillin was developed by adsorptive stripping voltammetry. Its determination was carried out at the anodically pre-treated boron-doped diamond electrode in aqueous solutions. Using square-wave stripping mode, the compound yielded a well-defined voltammetric
Chia-Lin Lee et al.
Journal of natural products, 72(9), 1568-1572 (2009-08-21)
Two new sesquiterpene coumarins, designated 5'-acetoxy-8'-hydroxyumbelliprenin (1) and 10'R-acetoxy-11'-hydroxyumbelliprenin (2), and a new diterpene, 15-hydroxy-6-en-dehydroabietic acid (3), along with 27 known compounds, were isolated from a CHCl(3)-soluble extract of Ferula assa-foetida through bioassay-guided fractionation. The structures of the new metabolites
Ana Rita Brochado et al.
Biotechnology and bioengineering, 110(2), 656-659 (2012-09-26)
Overproduction of a desired metabolite is often achieved via manipulation of the pathway directly leading to the product or through engineering of distant nodes within the metabolic network. Empirical examples illustrating the combined effect of these local and global strategies
Shixin Deng et al.
Journal of natural products, 69(4), 536-541 (2006-04-29)
Serotonin receptor (5-HT(7)) binding assay-directed fractionation of a methanol extract of the dried roots of Angelica sinensis led to the isolation and identification of 21 compounds including a new phenolic ester, angeliferulate (1), and three new phthalides, 10-angeloylbutylphthalide (2), sinaspirolide
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