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4-??????????

4-??????????
4-?????????? ??? ???
?? ??:
156-38-7
???:
4-??????????
???(??):
4-???????????;4-??????????
???:
4-Hydroxyphenylacetic acid
???(??):
2-(4-hydroxyphenyl)acetic acid;P-HYDROXYPHENYLACETIC ACID;PHPA;4-Hydroxybenzeneacetic acid;4-carboxymethylphenol;Benzeneacetic acid, 4-hydroxy-;4-Hydroxyphenylacetic;4-hydrophenylacetic acid;4-hydroxybenzeneaceticacid;NSC 27460
CBNumber:
CB6314323
???:
C8H8O3
??? ??:
152.15
MOL ??:
156-38-7.mol
MSDS ??:
SDS

4-?????????? ??

???
148-151 °C(lit.)
?? ?
234.6°C (rough estimate)
??
1.2143 (rough estimate)
???
0.007Pa at 25℃
???
1.4945 (estimate)
?? ??
Inert atmosphere,Room Temperature
???
50g/L
?? ?? (pKa)
4.50±0.10(Predicted)
??? ??
??? ??
??
???? ??? ?? ?? ???
??????(pH)
2.0-2.4 (30g/l, H2O, 20℃)
???
????????? ???? ?????. ?? ?? ?????.
BRN
1448766
InChI
1S/C8H8O3/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11)
InChIKey
XQXPVVBIMDBYFF-UHFFFAOYSA-N
SMILES
OC(=O)Cc1ccc(O)cc1
LogP
0.75 at 25℃
CAS ??????
156-38-7(CAS DataBase Reference)
NIST
Benzeneacetic acid, 4-hydroxy-(156-38-7)
EPA
Benzeneacetic acid, 4-hydroxy- (156-38-7)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xi
?? ???? ?? 36/37/38
????? 26-36-24/25
WGK ?? 3
RTECS ?? AI2680000
?? ?? ?? Irritant
TSCA TSCA listed
HS ?? 29182990
???? ??? 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
????(GHS): Exclamation Mark (GHS07)
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H315 ??? ??? ??? ????? ?? ????? ?? 2 ?? P264, P280, P302+P352, P321,P332+P313, P362
H319 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 2A ?? P264, P280, P305+P351+P338,P337+P313P
H335 ?? ???? ??? ? ?? ?? ???? ?? - 1? ??;???? ?? ?? 3 ??
??????:
P261 ??·?·??·???·??·...·????? ??? ????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
NFPA 704
1
2 0

4-?????????? MSDS


4-Hydroxyphenylacetic acid

4-?????????? C??? ??, ??, ??

??? ??

4-Hydroxyphenylacetic acid is a white to cream or light tan crystalline powder. sublimation. Insoluble in cold water, soluble in hot water, ether, ethanol, ethyl acetate. In the case of ferric chloride, it is a purple-green precipitate. It is used as a pharmaceutical raw material for the synthesis of cephalosporin antibiotics, antipyretic analgesics.

??

A compound present in olive oil. An important fine chemical intermediate with broad prospects for application development.

?? ??

4-Hydroxyphenylacetic acid is synthesized by diazotization and hydrolysis of 4-aminophenylacetic acid.
4-aminophenylacetic acid and alkali solution are prepared into sodium salt, and then sulfuric acid is added. Cool to 0°C, control the temperature at 0-5°C, and add sodium nitrate solution dropwise, and the reaction is completed for 0.5h. The obtained diazonium was added dropwise to dilute sulfuric acid at 90-95°C for about 1 hour, and the reaction was continued for 1 hour. The reaction solution was decolorized and filtered, cooled and extracted with ethyl acetate, and the extract was recovered with ethyl acetate to obtain 4-Hydroxyphenylacetic acid. The yield is about 85%.

??

ChEBI: 4-hydroxyphenylacetic acid is a monocarboxylic acid that is acetic acid in which one of the methyl hydrogens is substituted by a 4-hydroxyphenyl group. It has a role as a plant metabolite, a fungal metabolite, a human metabolite and a mouse metabolite. It is a monocarboxylic acid and a member of phenols. It derives from an acetic acid. It is a conjugate acid of a 4-hydroxyphenylacetate.

???? ??

4-Hydroxyphenylacetic acid (4-HPA) is an important microbial-derived metabolite of polyphenols in the intestinal tract[4].

Purification Methods

Crystallise the acid from water or Et2O/pet ether. The p-bromophenacyl ester has m 117o (from EtOH). [Beilstein 10 II 112, 10 III 430, 10 IV 543.]

4-?????????? ?? ?? ? ???

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?? ??


4-?????????? ?? ??

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4-?????????? ?? ??:

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