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About This Item
Linear Formula:
CH3C6H4CO2H
CAS Number:
Molecular Weight:
136.15
EC Number:
204-284-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1072103
MDL number:
InChI key
ZWLPBLYKEWSWPD-UHFFFAOYSA-N
InChI
1S/C8H8O2/c1-6-4-2-3-5-7(6)8(9)10/h2-5H,1H3,(H,9,10)
SMILES string
Cc1ccccc1C(O)=O
grade
puriss.
assay
≥99.5% (T)
ign. residue
≤0.05%
bp
258-259 °C (lit.)
mp
103-105 °C
density
1.062 g/mL at 25 °C (lit.)
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
298.4 °F - closed cup
flash_point_c
148 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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K H Wang et al.
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This investigation used UV light of 365 nm and titanium dioxide in aqueous suspension to study the photocatalytic reaction of o-methylbenzoic acid under the influence of pH values, anion additives and the varieties of titanium dioxide. From experimental results, under
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D Durkin et al.
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The concept of dual opposite injection in capillary electrophoresis (DOI-CE) for the simultaneous separation, under conditions of suppressed electroosmotic flow, of anionic and cationic compounds with no bias in resolution and analysis time, is extended to a higher pH range
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Mouse hepatic microsomal enzymes catalyzed the oxidation of o-, m-, and p-tolualdehydes, intermediate metabolites of xylene, to the corresponding toluic acids. Cofactor requirement for the catalytic activity indicates that the microsomes contain NAD- and NADPH-dependent enzymes for this reaction. GC/MS
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Aspirin has been proposed in recent years as a candidate for chemoprevention of adenocarcinoma in patients with Barrett's esophagus. The aim of the present study was to evaluate the effect of acetylsalicylic acid (ASA) in an experimental model of esophageal
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