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42183

Supelco

Melting point standard 182-184°C

analytical standard

Synonym(s):

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

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250 MG
¥3,030
1 G
¥10,180

¥3,030

Estimated to ship onMarch 27, 2025

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250 MG
¥3,030
1 G
¥10,180

About This Item

Linear Formula:
CH3OC6H4CO2H
CAS Number:
100-09-4
Molecular Weight:
152.15
Beilstein:
508910
EC Number:
202-818-5
MDL number:
MFCD00002542
UNSPSC Code:
20121904
PubChem Substance ID:
329756201
NACRES:
NA.24

¥3,030

Estimated to ship onMarch 27, 2025

Request a Bulk Order

grade

analytical standard

Quality Level

100

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

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

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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

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

365.0 °F - closed cup

Flash Point(C)

185 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

42183-VAR:
42183-1G:
42183-250MG:
42183-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL9593
BCCG0995
BCBW3902
BCCB7271
BCBW4727

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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
Patricia Ferreira et al.
The Journal of biological chemistry, 284(37), 24840-24847 (2009-07-04)
Aryl-alcohol oxidase (AAO) is a FAD-containing enzyme in the GMC (glucose-methanol-choline oxidase) family of oxidoreductases. AAO participates in fungal degradation of lignin, a process of high ecological and biotechnological relevance, by providing the hydrogen peroxide required by ligninolytic peroxidases. In
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
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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