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Key Documents

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W394505

Sigma-Aldrich

p-Anisic acid

≥99%, FG

Sinónimos:

4-Methoxybenzoic acid, p-Methoxybenzoic acid, Draconic acid

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About This Item

Fórmula lineal:
CH3OC6H4CO2H
Número de CAS:
100-09-4
Peso molecular:
152.15
FEMA Number:
3945
Beilstein/REAXYS Number:
508910
EC Number:
202-818-5
MDL number:
MFCD00002542
UNSPSC Code:
12164502
PubChem Substance ID:
24901946
Flavis number:
8.071
NACRES:
NA.21

biological source

synthetic

Quality Level

400

grade

FG
Fragrance grade

agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 110

assay

≥99%

mp

182-185 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

organoleptic

animal

SMILES string

COc1ccc(cc1)C(O)=O

InChI

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

InChI key

ZEYHEAKUIGZSGI-UHFFFAOYSA-N

Categorías relacionadas

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

365.0 °F - closed cup

flash_point_c

185 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
SHBR7597
SHBS1121
SHBP4575
SHBN9251
STBK1061

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Sigma-Aldrich

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9-Fluorenone 98%

Sigma-Aldrich

F1506

9-Fluorenone

2-Methoxybenzoic acid ReagentPlus®, 99%

Sigma-Aldrich

169978

2-Methoxybenzoic acid

trans-Stilbene 96%

Sigma-Aldrich

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trans-Stilbene

M Wessels et al.
Journal of natural products, 64(12), 1556-1558 (2002-01-05)
From the hydrophilic extract of the ascidian Polycarpa aurata three new compounds, N-(4-methoxybenzoyl)-N'-methylguanidine (1), butyl 2-(4-methoxyphenyl)-2-oxoacetate (2), and 2-(4-methoxyphenyl)-N-methyl-2-oxoacetamide (3), together with the known compounds methyl 2-(4-methoxyphenyl)-2-oxoacetate (4) and 4-methoxybenzoic acid were isolated. The structures of all isolates were determined
A Hage et al.
Applied microbiology and biotechnology, 52(6), 834-838 (2000-01-05)
Ligninolytic basidiomycetes were screened for their ability to reduce aryl acids to the corresponding aldehydes and alcohols. Seven fungal strains converted p-anisic acid in high molar yields to the reduced products. The white-rot fungus Bjerkandera sp. strain BOS55 was one
U Karlson et al.
Journal of bacteriology, 175(5), 1467-1474 (1993-03-01)
A red-pigmented coryneform bacterium, identified as Rhodococcus rhodochrous strain 116, that grew on 2-ethoxyphenol and 4-methoxybenzoate as sole carbon and energy sources was isolated. Phylogenetic analysis based on the 16S rDNA sequences indicates that the strain clusters more closely to
T Ogiso et al.
Journal of pharmaceutical sciences, 87(5), 594-598 (1998-05-20)
The pharmacokinetics of aniracetam (AP), a new cognitive performance enhancer, and its main metabolites was investigated after intravenous (iv) and oral administrations to rat. The plasma levels of AP, 4-p-anisamidobutyric acid (ABA), and p-anisic acid (AA) were determined simultaneously by
C Gadgoli et al.
Journal of ethnopharmacology, 66(2), 187-192 (1999-08-05)
p-Methoxy benzoic acid isolated from the methanolic soluble fraction of the aqueous extract of Capparis spinosa L. (Capparidaceae) was found to possess significant antihepatotoxic activity against carbontetrachloride and paracetamol induced hepatotoxicity in vivo and thioacetamide and galactosamine induced hepatotoxicity in
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