Skip to Content
MilliporeSigma
All Photos(1)

Documents

117390

Sigma-Aldrich

4-Methoxybenzoic acid

ReagentPlus®, 99%

Synonym(s):

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

Sign Into View Organizational & Contract Pricing
All Photos(1)

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:
12352100
eCl@ss:
39023905
PubChem Substance ID:
24847329
NACRES:
NA.22

product line

ReagentPlus®

Assay

99%

mp

182-185 °C (lit.)

solubility

H2O: soluble 2500 parts
alcohol: freely soluble
boiling water: soluble
chloroform: freely soluble
diethyl ether: freely soluble
ethyl acetate: freely soluble

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

Looking for similar products? Visit Product Comparison Guide

General description

4-Methoxybenzoic acid is the sole source of carbon and energy for growth in the cultures of Nocardia sp. DSM 1069.

Application

4-Methoxybenzoic acid was used in oxidation and reduction of cytochrome c in solution through different self-assembled monolayers on gold electrodes using cyclic voltammetry.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Control of the electron transfer rate between cytochrome c and gold electrodes by the manipulation of the electrode's hydrogen bonding character.
Liu H, et al.
Langmuir, 19(6), 2378-2387 (2003)
Degradation of coniferyl alcohol and other lignin-related aromatic compounds by Nocardia sp. DSM 1069.
Eggeling L and Sahm H.
Archives of Microbiology, 126(2), 141-148 (1980)
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
K Sekar et al.
Acta crystallographica. Section D, Biological crystallography, 62(Pt 4), 392-397 (2006-03-23)
The lipolytic enzyme phospholipase A2 plays a crucial role in lipid metabolism and catalyzes hydrolysis of the fatty-acid ester bond at the sn-2 position of phospholipids. Here, the crystal structure (1.7 A resolution) of the triple mutant (K53,56,121M) of bovine
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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service