4-Hydroxyphenoxyacetic Acid
Names
[ CAS No. ]:
1878-84-8
[ Name ]:
4-Hydroxyphenoxyacetic Acid
[Synonym ]:
4-(Carboxymethoxy)phenol
(4-hydroxy-phenoxy)-acetic acid
MFCD00014362
p-hydroxy-phenoxyacetic acid
Hydrochinon-mono-glykolsaeure
4-Hydroxypheoxyacetate
EINECS 217-525-8
(4-Hydroxyphenoxy)acetic acid
(4-Hydroxy-phenoxy)-essigsaeure
Acetic acid,(4-hydroxyphenoxy)
4-Hydroxyphenoxyacetic Acid
Chemical & Physical Properties
[ Density]:
1.367g/cm3
[ Boiling Point ]:
372.6ºC at 760mmHg
[ Melting Point ]:
154-157 °C(lit.)
[ Molecular Formula ]:
C8H8O4
[ Molecular Weight ]:
168.14700
[ Flash Point ]:
158.3ºC
[ Exact Mass ]:
168.04200
[ PSA ]:
66.76000
[ LogP ]:
0.85560
[ Vapour Pressure ]:
3.27E-06mmHg at 25°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Articles
Colloids Surf. B Biointerfaces 102 , 95-101, (2013)
Individual dispersion of single-walled carbon nanotubes (SWNTs) in biocompatible media is of particular interest for diverse biomedical and nanomedicine applications. Herein we present, for the first ...
A synthetic heparin-mimicking polyanionic compound binds to the LDL receptor-related protein and inhibits vascular smooth muscle cell proliferation.J. Cell. Biochem. 81(1) , 114-27, (2001)
A synthetic heparin-mimicking polyaromatic anionic compound RG-13577 (polymer of 4-hydroxyphenoxy acetic acid and formaldehyde ammonium salt, Mr approximately 5800) exhibits specific binding to vascul...
Design, synthesis, and evaluation of postulated transient intermediate and substrate analogues as inhibitors of 4-hydroxyphenylpyruvate dioxygenase.Bioorg. Med. Chem. Lett. 12(13) , 1709-13, (2002)
An epoxybenzoquinone, 4-hydroxyphenoxypropionic acid, and 2-hydroxy-3-phenyl-3-butenoic acid derivatives have been designed, synthesized, and evaluated for in vitro inhibition activity against 4-hydro...