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42183

Supelco

Melting point standard 182.5-184.5°C

analytical standard

Sinonimo/i:

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

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About This Item

Formula condensata:
CH3OC6H4CO2H
Numero CAS:
100-09-4
Peso molecolare:
152.15
Beilstein:
508910
Numero CE:
202-818-5
Numero MDL:
MFCD00002542
Codice UNSPSC:
20121904
ID PubChem:
329756201
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Durata

limited shelf life, expiry date on the label

Punto di fusione

182-184 °C (±0.3°C)
182-185 °C (lit.)

applicazioni

food and beverages
pharmaceutical

Formato

neat

Stringa SMILE

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)
ZEYHEAKUIGZSGI-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

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.

Applicazioni

This product is an analytical standard used as a melting point calibration standard.

Caratteristiche e vantaggi

  • 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

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

365.0 °F - closed cup

Punto d’infiammabilità (°C)

185 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCL9593
BCCG0995
BCBW3902
BCCB7271
BCBW4727

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Supelco

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4-Methoxybenzoic acid for synthesis

Sigma-Aldrich

8.05971

4-Methoxybenzoic acid

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
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
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
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