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393819

4-Acetylphenoxyacetic acid

Name: 4-Acetylphenoxyacetic acid
Brand: ALDRICH

99%

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About This Item

Linear Formula:

CH₃COC₆H₄OCH₂CO₂H

CAS Number:

1878-81-5

Molecular Weight:

194.18

NACRES:

NA.22

PubChem Substance ID:

24864544

UNSPSC Code:

12352100

EC Number:

217-524-2

MDL number:

MFCD00014363

Assay:

99%

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Properties

assay

99%

mp

175-177 °C (dec.) (lit.)

solubility

methanol: soluble 25 mg/mL, clear, colorless to faintly yellow

functional group

carboxylic acid, ketone

SMILES string

CC(=O)c1ccc(OCC(O)=O)cc1

InChI

1S/C10H10O4/c1-7(11)8-2-4-9(5-3-8)14-6-10(12)13/h2-5H,6H2,1H3,(H,12,13)

InChI key

KMXZEXUYXUMHEQ-UHFFFAOYSA-N

Description

General description

4-Acetylphenoxyacetic acid is a phenoxyacetic acid derivative. It has been synthesized by employing para-acetyl phenol as starting reagent.

Application

4-Acetylphenoxyacetic acid is suitable as a test compound in the study of phenylacetic acid transport system (PATS) of Pseudomonas putida U by the aerobic catabolism of phenylacetic acid derivative used as the sole carbon source.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Aerobic catabolism of phenylacetic acid in Pseudomonas putida U: biochemical characterization of a specific phenylacetic acid transport system and formal demonstration that phenylacetyl-coenzyme A is a catabolic intermediate.

C Schleissner et al.

Journal of bacteriology, 176(24), 7667-7676 (1994-12-01)

The phenylacetic acid transport system (PATS) of Pseudomonas putida U was studied after this bacterium was cultured in a chemically defined medium containing phenylacetic acid (PA) as the sole carbon source. Kinetic measurement was carried out, in vivo, at 30

Photocyclization reactions. Part 1. Synthesis of dihydrobenzofuranols using photocyclization of 2-alkoxybenzaldehydes, 2'-alkoxyacetophenones, 2-formylphenoxyacetic acids and 2-acetylphenoxyacetic acids

Horaguchi T, et al.

Journal of Heterocyclic Chemistry, 28(5), 1261-1272 (1991)

Design of new potent hypolipidemic agents with the synergistic structural properties of α-asarone and fibrates.

Zuniga C, et al.

Drug Development Research, 64(1), 28-40 (2005)

Global Trade Item Number

SKU	GTIN
393819-5G	04061831820096