42183
Melting point standard 182.5-184.5°C
analytical standard
Synonyme(s) :
p-Anisic acid, 4-Methoxybenzoic acid, p-Methoxybenzoic acid, Draconic acid
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A propos de cet article
Formule linéaire :
CH3OC6H4CO2H
Numéro CAS:
Poids moléculaire :
152.15
UNSPSC Code:
20121904
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-818-5
Beilstein/REAXYS Number:
508910
MDL number:
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Laissez-nous vous aiderInChI
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
InChI key
ZEYHEAKUIGZSGI-UHFFFAOYSA-N
grade
analytical standard
shelf life
limited shelf life, expiry date on the label
mp
182-184 °C (±0.3°C), 182-185 °C (lit.)
application(s)
food and beverages
pharmaceutical
format
neat
Quality Level
Catégories apparentées
General description
Melting point standard 182-184 °C, p-anisic acid is useful for the regular assessment of identity or purity of a substance. Its value is determined as an average of 6 to 12 measurements with a Büchi B-545 instrument that is calibrated against primary standards.
Application
This product is an analytical standard used as a melting point calibration standard.
Features and Benefits
- Traceable to primary standards from LGC, London
- Grade: Analytical Standard
- Melting point standardized in the thermodynamic mode of analysis
- Standard deviation up to ± 0.3 °C
- Documented with certificates of analysis and safety data sheet
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
Classe de stockage
11 - Combustible Solids
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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
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
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
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
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
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