4-methoxyphenyl acetic acid
acetic acid, 4-methoxyphenyl-
Identification
| Name | 4-methoxyphenyl acetic acid |
| IUPAC | 2-(4-methoxyphenyl)acetic acid |
| CAS Number | 104-01-8 |
| EINECS | 203-166-4 |
| FDA UNII | AJP2V8U5K6 |
| Molecular Formula | C9 H10 O3 |
| Molecular Weight | 166.17630000 |
| MDL Number | MFCD00004345 |
| Nikkaji Number | J10.116H |
| Beilstein | 1101737 |
| XlogP3 | 1.40 (est) |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Melting Point | 87.00 °C. @ 760.00 mm Hg |
| Boiling Point | 138.00 to 140.00 °C. @ 3.00 mm Hg, 306.00 to 307.00 °C. @ 760.00 mm Hg (est) |
| Vapor Pressure | 0.000345 mmHg @ 25.00 °C. (est) |
| Flash Point | 256.00 °F. TCC ( 124.30 °C. ) (est) |
| logP (o/w) | 1.420 |
| Soluble in | alcohol |
| Insoluble in | water |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | oral-rat LD50 1550 mg/kg |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | herbicides / pesticides |
| Recommendation for 4-methoxyphenyl acetic acid usage levels up to | not for fragrance use. |
| Recommendation for 4-methoxyphenyl acetic acid flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
acetic acid, (p-methoxyphenyl)-
acetic acid, 4-methoxyphenyl-
acetic acid, p-methoxyphenyl-
homo
anisic acid
homo-p-
anisic acid
2-(p-
anisyl)acetic acid
2-(para-
anisyl)acetic acid
benzeneacetic acid, 4-methoxy-
4-
methoxy phenylacetic acid
p-
methoxy-a-toluic acid
4-
methoxy-benzeneacetic acid
(4-
methoxy-phenyl)-acetic acid
4-
methoxybenzeneacetic acid
p-
methoxyphenyl-acetic acid
(4-
methoxyphenyl)acetic acid
(p-
methoxyphenyl)acetic acid
2-(4-
methoxyphenyl)acetic acid
4-
methoxyphenylacetic acid
p-
methoxyphenylacetic acid
4-
methoxyphenylaceticacid
PubMed:
Synthesis and evaluation of the cytotoxicity of a series of 1,3,4-thiadiazole based compounds as anticancer agents.
PubMed:
Anticancer activity of dinuclear gallium(III) carboxylate complexes.
PubMed:
Characterization of pu-erh tea using chemical and metabolic profiling approaches.
PubMed:
Design and synthesis of 4-methoxyphenylacetic acid esters as 15-lipoxygenase inhibitors and SAR comparative studies of them.
PubMed:
Determination of selected neurotransmitter metabolites using monolithic column chromatography coupled with chemiluminescence detection.
PubMed:
Coenzyme Q0 induces apoptosis and modulates the cell cycle in estrogen receptor negative breast cancer cells.
PubMed:
Study of the cytotoxic activity of di and triphenyltin(IV) carboxylate complexes.
PubMed:
15N CIDNP investigations of the peroxynitric acid nitration of L-tyrosine and of related compounds.
PubMed:
Bromophenol derivatives from the red alga Rhodomela confervoides.
PubMed:
Development and substantiation of a liquid chromatographic method for monitoring organic reactions involved in synthesis of 4-methoxyphenylacetic acid.
PubMed:
Syntheses and in vitro evaluation of 4-(2-aminoethyl)-2(3H)-indolones and related compounds as peripheral prejunctional dopamine receptor agonists.
PubMed:
[Microbial degradation of papaverine (author's transl)].
PubMed:
Metabolism of 3, 4-dihydroxyphenylalanine, its metabolites and analogues in vivo in the rat: urinary excretion pattern.
PubMed:
The estimation of 3,4-dihydroxyphenylacetic acid, homovanillic acid and homo-isovanillic acid in nervous tissue by gas-liquid chromatography and electron capture detection.
PubMed:
[4-O-Methylated catecholamines: 3-hydroxy, 4-methoxyphenylacetic acid (homo-isovanillic acid, iso-HVA) in biological media: urine, cerebrospinal fluid, and brain tissue].
PubMed:
The 4-0-methyl metabolites of catecholamines in man: chromatographic identification of 3-hydroxy,4-methoxyphenylacetic acid (homo-iso-vanillic acid) in cerebrospinal fluid.
PubMed:
[Attempted cyclization of 5-substituted-2-(5-carboxymethyl-2-methoxyphenoxy)-4-methoxyphenylacetic acid with polyphosphoris acid (studies on the synthesis of heterocyclic compounds. CCXLII].