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Merck

W394505

p-Anisic acid

≥99%, FG

Sinónimos:

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

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Acerca de este artículo

Fórmula lineal:
CH3OC6H4CO2H
Número CAS:
Peso molecular:
152.15
Flavis number:
8.071
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
3945
NACRES:
NA.21
EC Number:
202-818-5
MDL number:
Beilstein/REAXYS Number:
508910
Organoleptic:
animal
Grade:
FG, Fragrance grade
Biological source:
synthetic
Agency:
follows IFRA guidelines
Food allergen:
no known allergens
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InChI key

ZEYHEAKUIGZSGI-UHFFFAOYSA-N

InChI

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

SMILES string

COc1ccc(cc1)C(O)=O

biological source

synthetic

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%

Quality Level

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

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Categorías relacionadas

Clase de almacenamiento

11 - Combustible Solids

wgk

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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Stephen G Bell et al.
Dalton transactions (Cambridge, England : 2003), 41(28), 8703-8714 (2012-06-15)
The crystal structures of the 4-methoxybenzoate bound forms of cytochrome P450 enzymes CYP199A2 and CYP199A4 from the Rhodopseudomonas palustris strains CGA009 and HaA2 have been solved. The structures of these two enzymes, which share 86% sequence identity, are very similar
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
N Chaves et al.
Journal of chemical ecology, 27(3), 611-621 (2001-07-10)
Eleven allelochemicals (ferulic acid, cinnamic acid, 4-hydroxybenzoic acid, hydroxycinnamic acid, methyl propionate, oxalic acid, methylmalonic acid, p-anisic acid, butyric acid, 3-hydroxybutyric acid, and azulene) were identified in the exudate of Cistus ladanifer L. We studied the effect of each on
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
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

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