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Merck

34366

Phenoxyacetic acid

PESTANAL®, analytical standard

Synonym(s):

Glycolic acid phenyl ether

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About This Item

Linear Formula:
C6H5OCH2CO2H
CAS Number:
122-59-8
Molecular Weight:
152.15
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329754966
EC Number:
204-556-7
Beilstein/REAXYS Number:
907949
MDL number:
MFCD00004296

Product Name

Phenoxyacetic acid, PESTANAL®, analytical standard

InChI key

LCPDWSOZIOUXRV-UHFFFAOYSA-N

InChI

1S/C8H8O3/c9-8(10)6-11-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)

SMILES string

OC(=O)COc1ccccc1

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

98-100 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - 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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK2865
BCBZ9082

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Huiting Zhang et al.
Bioorganic & medicinal chemistry, 15(18), 6089-6095 (2007-07-07)
Molecular imprinted polymers (MIPs) binding with phenoxyacetic acid (PA) as a dummy template molecule were synthesized via thermal initiation in aqueous medium. The retention behaviors of benzoic acid (BA), PA, 2-methyl-4-chlorophenoxyacetic acid (MCPA), 4-chlorophenoxyacetic acid (4-CPA), and 2,4-dichlorophenoxyacetic acid (2,4-D)
Ming-Kung Yeh et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 27(1), 49-54 (2011-01-15)
Dynamic liquid-liquid-liquid microextraction coupled with ion-pair liquid chromatography (IP-LC) and photodiode array detection was developed and used for the extraction and analysis of chlorinated phenoxyacetic acids (CPAs) and chlorophenols (CPs) from water samples. An organic extraction solvent mixture was chosen
Guan-Sheng Jiao et al.
Bioorganic & medicinal chemistry letters, 22(6), 2242-2246 (2012-02-22)
Four core structures capable of providing sub-nanomolar inhibitors of anthrax lethal factor (LF) were evaluated by comparing the potential for toxicity, physicochemical properties, in vitro ADME profiles, and relative efficacy in a rat lethal toxin (LT) model of LF intoxication.
Giuseppe Fracchiolla et al.
ChemMedChem, 2(5), 641-654 (2007-03-16)
Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors that govern lipid and glucose homeostasis, and play a central role in cardiovascular disease, obesity, and diabetes. Thus, there is significant interest in developing new and specific agonists for these receptors. Herein
Mohamed Ashraf Ali et al.
Bioorganic & medicinal chemistry, 15(5), 1896-1902 (2007-01-26)
A series of 2-{4-[1-amino (thioxo) methyl-5-(substituted phenyl)-4,5-dihydro-1H-3-pyrazolyl]-2-methoxyphenoxy}acetic acid and 2-{4-[1-carbamoyl-5-(substituted phenyl)-4,5-dihydro-1H-3-pyrazolyl]-2-methoxyphenoxy}acetic acid were synthesized and the in vitro activity of the synthesized compounds against Mycobacterium tuberculosis H37Rv (MTB) and INH-resistant M. tuberculosis (INHR-MTB) was studied. Among the synthesized compounds, compound
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