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34366

Phenoxyessigsäure

Name: Phenoxyessigsäure
Brand: SIAL

PESTANAL^®, analytical standard

Synonym(e):

Glycolsäurephenylether

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Packungsgröße	SKU	Verfügbarkeit	Preis

Über diesen Artikel

Lineare Formel:

C₆H₅OCH₂CO₂H

CAS-Nummer:

122-59-8

Molekulargewicht:

152.15

UNSPSC Code:

41116107

NACRES:

NA.24

PubChem Substance ID:

329754966

EC Number:

204-556-7

Beilstein/REAXYS Number:

907949

MDL number:

MFCD00004296

Preise und Verfügbarkeit sind derzeit nicht verfügbar.

Technischer Dienst

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Unterstützung erhalten

Eigenschaften

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

SMILES string

OC(=O)COc1ccccc1

InChI

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

InChI key

LCPDWSOZIOUXRV-UHFFFAOYSA-N

Beschreibung

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

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Dieser Artikel	61074	53877	92264
Supelco 34366 Phenoxyacetic acid	Supelco 61074 Propiophenone	Supelco 53877 2,6-Dimethoxyphenol	Supelco 92264 4-Methoxyphenol
application(s) agriculture cleaning products cosmetics environmental flavors and fragrances food and beverages personal care	application(s) cleaning products cosmetics flavors and fragrances food and beverages personal care	application(s) cleaning products cosmetics flavors and fragrances food and beverages personal care	application(s) cleaning products cosmetics environmental flavors and fragrances food and beverages personal care
technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable	technique(s) HPLC: suitable, gas chromatography (GC): suitable
format neat	format neat	format neat	format neat
grade analytical standard	grade analytical standard	grade analytical standard	grade analytical standard
shelf life limited shelf life, expiry date on the label	shelf life limited shelf life, expiry date on the label	shelf life limited shelf life, expiry date on the label	shelf life limited shelf life, expiry date on the label
mp 98-100 °C (lit.)	mp 17-19 °C (lit.)	mp 50-57 °C (lit.), 53-57 °C	mp 55-57 °C (lit.)

Still not finding the right product?

Explore all of our products under Phenoxyessigsäure

pictograms

GHS07

signalword

Warning

hcodes

H302,H315,H319,H335

pcodes

P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

BCCK2865

BCBZ9082

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Synthesis and evaluation of in vitro antiviral activity of novel phenoxy acetic acid derivatives.

M Shahar Yar et al.

Journal of enzyme inhibition and medicinal chemistry, 24(3), 876-882 (2008-10-28)

Several substituted phenoxy acetic acid derived pyrazolines were synthesized by the reaction between 2-{4-[3-(2,4-dihydroxyphenyl)-3-oxo-1-propenyl]-2-methoxyphenoxy} acetic acid and substituted acid hydrazides and were tested for their in vitro cytotoxicity and antiviral activity. None of the compounds showed any specific antiviral activity

Discovery of novel phenoxyacetic acid derivatives as antimycobacterial agents.

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

Phenoxyacetic acids as PPARδ partial agonists: synthesis, optimization, and in vivo efficacy.

Karen A Evans et al.

Bioorganic & medicinal chemistry letters, 21(8), 2345-2350 (2011-03-19)

A series of phenoxyacetic acids as subtype selective and potent hPPARδ partial agonists is described. Many analogues were readily accessible via a single solution-phase synthetic route which resulted in the rapid identification of key structure-activity relationships (SAR), and the discovery