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Key Documents

W398802

Sigma-Aldrich

Vanillic acid

≥97%, FG

Sinonimo/i:

4-Hydroxy-3-methoxybenzoic acid

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About This Item

Formula condensata:
HOC6H3(OCH3)CO2H
Numero CAS:
Peso molecolare:
168.15
Numero FEMA:
3988
Beilstein:
2208364
Numero CE:
Numero MDL:
Codice UNSPSC:
12164502
ID PubChem:
Numero Flavis:
8.043
NACRES:
NA.21

Origine biologica

synthetic

Livello qualitativo

Grado

FG
Halal
Kosher

Conformità normativa

EU Regulation 1334/2008 & 178/2002

Saggio

≥97%

Punto di fusione

208-210 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Organolettico

creamy; milk; sweet; vanilla

Stringa SMILE

COc1cc(ccc1O)C(O)=O

InChI

1S/C8H8O4/c1-12-7-4-5(8(10)11)2-3-6(7)9/h2-4,9H,1H3,(H,10,11)
WKOLLVMJNQIZCI-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Natural occurrence: Guava, grape, brandy, rum, whiskey, sherry, red and white wines, Scotch and Canadian whiskey.
Vanillic acid is one of the key aromatic volatile compounds of vanilla beans.

Applicazioni

Vanillic acid is a phenolic derivative, which is generally used as a flavoring agent in food products. It can be used in the synthesis of a well-known flavoring agent vanillin.

Azioni biochim/fisiol

Odor at 5%
Taste at 100 ppm

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


Certificati d'analisi (COA)

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Sigma-Aldrich

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Sigma-Aldrich

W310727

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Sigma-Aldrich

V1104

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Sigma-Aldrich

163333

Geraniol

Solid-liquid phase equilibrium and thermodynamic properties of vanillic acid in different pure solvents
Noubigh A and Abderrabba M
Journal of Molecular Liquids, 223, 261-266 (2016)
Vanillin and related flavor compounds in vanilla extracts made from beans of various global origins
Ranadive AS.
Journal of Agricultural and Food Chemistry, 40(10), 1922-1924 (1992)
Delphine Lamoral-Theys et al.
Bioorganic & medicinal chemistry, 18(11), 3823-3833 (2010-05-15)
A series of 33 novel divanillates and trivanillates were synthesized and found to possess promising cytostatic rather than cytotoxic properties. Several compounds under study decreased by >50% the activity of Aurora A, B, and C, and WEE1 kinase activity at
B L Lee et al.
Clinical chemistry, 39(9), 1788-1792 (1993-09-01)
We describe a sensitive and specific high-performance liquid-chromatographic method for determining the benzene metabolite, trans,trans-muconic acid (ttMA) in urine by measuring ultraviolet absorbance at 265 nm. We mix 1 mL of urine sample with 2 mL of Tris buffer containing
F Mashige et al.
Journal of chromatography. B, Biomedical applications, 658(1), 63-68 (1994-08-05)
An HPLC system for the simultaneous determination of acidic catecholamine metabolites, related compounds and 5-hydroxyindoleacetic acid (5-HIAA) in human urine was developed. A mixed-mode (C18/anion-exchange) column with isocratic elution using citrate buffer and an eight-channel electrochemical detector were used. Vanilmandelic

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