3-Methoxyphenylacetic acid
3-Methoxyphenylacetic acid
  • CAS No.:1798-09-0
Other grades of this product :
3-Methoxyphenylacetic acid Basic information
Product Name:3-Methoxyphenylacetic acid
Synonyms:3-Methoxybenzeneacetic acid;3-methoxy-benzeneaceticaci;3-methoxybenzeneaceticacid;Acetic acid, (m-methoxyphenyl)-;Benzeneaceticacid,3-methoxy-;m-Methoxyphenylessigsαure;m-Methoxyphenylacetic acid, P-Methoxyphenylacetic acid, Anisylacetic acid, m-OMePAA;3-Methoxyphenylessigsure
CAS:1798-09-0
MF:C9H10O3
MW:166.17
EINECS:217-282-8
Product Categories:Building Blocks;Carbonyl Compounds;Aromatic Phenylacetic Acids and Derivatives;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks;Acids and Derivatives;Phenyls & Phenyl-Het;Aromatics;Carboxylic Acids;Phenyls & Phenyl-Het;C9;Carbonyl Compounds
Mol File:1798-09-0.mol
3-Methoxyphenylacetic acid Chemical Properties
Melting point 65-69 °C (lit.)
Boiling point 306 °C
density 1.1708 (rough estimate)
refractive index 1.5500 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Soluble in Chloroform and Ethyl Acetate.
form Flakes
pka4.19±0.10(Predicted)
color White to slightly yellow
Water Solubility SLIGHTLY SOLUBLE
BRN 2614004
CAS DataBase Reference1798-09-0(CAS DataBase Reference)
NIST Chemistry ReferenceBenzeneacetic acid, 3-methoxy-(1798-09-0)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
RTECS AI8940000
HazardClass IRRITANT
HS Code 29189090
MSDS Information
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3-Methoxyphenylacetic acid English
SigmaAldrich English
ACROS English
ALFA English
3-Methoxyphenylacetic acid Usage And Synthesis
Chemical PropertiesOff-White Solid
UsesA fluorimetric method for the estimation of 4-hydroxy-3-methoxyphenylacetic acid (homovanillic acid) has been developed and applied to normal brain tissue. The presence of homovanillic acid in the caudate nucleus of normal animals of several species has been demonstrated.
Purification MethodsCrystallise the acid from H2O, or aqueous EtOH. The S-benzylisothiuronium salt has m 160-161o (from EtOH). [Beilstein 10 I 82, 10 III 428, 10 IV 541.]

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