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4-Methoxyphenoxyacetic acid

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4-Methoxyphenoxyacetic acid manufacturers

4-Methoxyphenoxyacetic acid Basic information
Product Name:4-Methoxyphenoxyacetic acid
Synonyms:RARECHEM AL BO 0321;(P-METHOXYPHENOXY)ACETIC ACID;2-(4-methoxyphenoxy)acetate;4-Methoxyphenoxyacetic acid, 98+%;4-Methoxyphenyloxyacetic acid;4-Methoxyphenoxyacetic acid,97%;2-(4-methoxyphenoxy)ethanoic acid;Acetic acid, (4-methoxyphenoxy)-
CAS:1877-75-4
MF:C9H10O4
MW:182.17
EINECS:217-513-2
Product Categories:Phenoxyacetic Acids and Alcohols (substituted);Organic acids
Mol File:1877-75-4.mol
4-Methoxyphenoxyacetic acid Structure
4-Methoxyphenoxyacetic acid Chemical Properties
Melting point 112-114 °C
Boiling point 275.56°C (rough estimate)
density 1.2481 (rough estimate)
refractive index 1.4345 (estimate)
storage temp. Sealed in dry,Room Temperature
pkapK1:3.213 (25°C)
AppearanceOff-white to light brown Solid
BRN 1874579
InChIInChI=1S/C9H10O4/c1-12-7-2-4-8(5-3-7)13-6-9(10)11/h2-5H,6H2,1H3,(H,10,11)
InChIKeyBHFSBJHPPFJCOS-UHFFFAOYSA-N
SMILESC(O)(=O)COC1=CC=C(OC)C=C1
CAS DataBase Reference1877-75-4(CAS DataBase Reference)
NIST Chemistry ReferenceAcetic acid, (4-methoxyphenoxy)-(1877-75-4)
EPA Substance Registry SystemAcetic acid, (4-methoxyphenoxy)- (1877-75-4)
Safety Information
Hazard Codes Xi
Risk Statements 44-36/37/38
Safety Statements 37/39-26
TSCA TSCA listed
HazardClass IRRITANT
HS Code 29189990
MSDS Information
ProviderLanguage
4-Methoxyphenoxyacetic acid English
ACROS English
ALFA English
4-Methoxyphenoxyacetic acid Usage And Synthesis
Chemical PropertiesBEIGE-BROWN CRYSTALLINE SOLID
Uses2-(4-Methoxyphenoxy)acetic Acid is a useful research chemical, a metabolite of mefexamide in human urine samples.
Synthesis
4-Methoxyphenol

150-76-5

Chloroacetic acid

79-11-8

4-Methoxyphenoxyacetic acid

1877-75-4

Compounds B1-7 were prepared by similar methods. In the synthesis of B1, monochloroacetic acid (0.04 mol, 3.78 g) was first dissolved in 15 mL of deionized water under stirring and ice bath conditions. Subsequently, 25% NaOH solution was added drop by drop and the pH was adjusted to 9-10 to produce sodium chloroacetate solution. In another vessel, NaOH (0.03 mol, 1.20 g), 15 mL of deionized water, 5 mL of ethanol and phenol (0.04 mol, 3.76 g) were mixed, and the above sodium chloroacetate solution was added slowly with stirring. After addition, stirring was continued for 20 minutes, followed by dropwise addition of sodium chloroacetate solution and the reaction mixture was heated to 105 °C and refluxed for 5 hours. After completion of the reaction, the mixture was cooled to room temperature and acidified with dilute hydrochloric acid to pH 1-2. The precipitate was collected by filtration, washed several times with dilute hydrochloric acid, and after recrystallization and drying in vacuum, the white solid product phenoxyacetic acid (B1) was obtained.

References[1] Synthetic Communications, 1996, vol. 26, # 23, p. 4337 - 4341
[2] Journal of Fluorescence, 2015, vol. 25, # 4, p. 849 - 859
[3] Luminescence, 2018, vol. 33, # 5, p. 855 - 862
[4] Luminescence, 2015, vol. 30, # 5, p. 677 - 685
[5] Journal of Molecular Structure, 2014, vol. 1074, p. 487 - 495
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