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4-HYDROXYPHENOXYACETIC ACID

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4-HYDROXYPHENOXYACETIC ACID Basic information

Product Name:
4-HYDROXYPHENOXYACETIC ACID
Synonyms:
  • 4-HYDROXYPHENOXYACETIC ACID
  • 2-(4-Hydroxyphenoxy)acetic acid
  • 2-(4-Hydroxyphenoxy)ethanoic acid, 4-(Carboxymethoxy)phenol
  • (P-HYDROXYPHENOXY)ACETIC ACID
  • (4-hydroxyphenoxy)-aceticaci
  • 4-Hydroxyphenoxyacetic acid, 98+%
  • Acetic acid, 2-(4-hydroxyphenoxy)-
  • 2-(4-hydroxyphenoxy)aceticaci
CAS:
1878-84-8
MF:
C8H8O4
MW:
168.15
EINECS:
217-525-8
Product Categories:
  • Phenoxyacetic Acids and Alcohols (substituted)
  • Carbonyl Compounds
  • C8
  • Carboxylic Acids
Mol File:
1878-84-8.mol
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4-HYDROXYPHENOXYACETIC ACID Chemical Properties

Melting point:
154-157 °C (lit.)
Boiling point:
372.6±17.0 °C(Predicted)
Density 
1.367±0.06 g/cm3(Predicted)
solubility 
soluble in Methanol
form 
Fine Crystalline Powder
pka
3.27±0.10(Predicted)
color 
Off-white to beige
BRN 
1952779
LogP
0.650
CAS DataBase Reference
1878-84-8(CAS DataBase Reference)
EPA Substance Registry System
Acetic acid, (4-hydroxyphenoxy)- (1878-84-8)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
TSCA 
Yes
HS Code 
29189990

MSDS

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4-HYDROXYPHENOXYACETIC ACID Usage And Synthesis

Chemical Properties

off-white to beige fine crystalline powder

Uses

2-(4-Hydroxyphenoxy)acetic Acid is used in the design, synthesis and evaluation of postulated transient intermediate and substrate analogues as inhibitors of 4-hyroxyphenylpyruvate dioxygenase. Acts as a reagent in the preparation, anti-HIV and kinesin Eg5 inhibitory activities, QSAR, and modeling studies of triazolothiadiazole and triazolothiadiazine derivatives. Synthesis of thiadiazolotriazin-4-ones and study of their mosquito-larvicidal and antibacterial properties.

Definition

ChEBI: 4-Hydroxypheoxyacetate is a monocarboxylic acid.

General Description

(4-Hydroxyphenoxy)acetic acid along with formaldehyde ammonium salt forms a polyaromatic anionic compound RG-13577. RG-13577 mimics the synthetic heparin and specifically binds to the vascular smooth muscle cells (SMCs) and inhibits their proliferative growth. In the molecules of (4-hydroxyphenoxy)acetic acid, the carboxyl groups are held together by R22(8) hydrogen bonds.

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