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233013

2-(3-Chlorophenoxy)propionic acid

Name: 2-(3-Chlorophenoxy)propionic acid
Brand: ALDRICH

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About This Item

Linear Formula:

CH₃CH(OC₆H₄Cl)CO₂H

CAS Number:

101-10-0

Molecular Weight:

200.62

NACRES:

NA.22

PubChem Substance ID:

24853946

UNSPSC Code:

12352100

EC Number:

202-915-2

MDL number:

MFCD00009723

Assay:

98%

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Properties

Quality Level

100

assay

98%

mp

113-115 °C (lit.)

functional group

carboxylic acid, chloro

SMILES string

CC(Oc1cccc(Cl)c1)C(O)=O

InChI

1S/C9H9ClO3/c1-6(9(11)12)13-8-4-2-3-7(10)5-8/h2-6H,1H3,(H,11,12)

InChI key

YNTJKQDWYXUTLZ-UHFFFAOYSA-N

Description

General description

2-(3-Chlorophenoxy)propionic acid is a chiral phenoxy acid herbicide. Enantiomeric resolution of 2-(3-chlorophenoxy)propionic acid has been performed by electrokinetic chromatography using a cyclodextrin as chiral pseudophase (CD-EKC).

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

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Enantiomeric separation of chiral phenoxy acid herbicides by electrokinetic chromatography. Application to the determination of analyte-selector apparent binding constants for enantiomers.

Y Martín-Biosca et al.

Electrophoresis, 22(15), 3216-3225 (2001-10-09)

The enantiomeric resolution of chiral phenoxy acid herbicides was performed by electrokinetic chromatography using a cyclodextrin as chiral pseudophase (CD-EKC). A systematic evaluation of several neutral and charged cyclodextrins was made. Among the cyclodextrins tested, (2-hydroxy)propyl beta-cyclodextrin (HP-beta-CD) was found

Separation of enantiomers of chiral weak acids with polysaccharide-based chiral columns and aqueous-organic mobile phases in high-performance liquid chromatography: Typical reversed-phase behavior?

Iza Matarashvili et al.

Journal of chromatography. A, 1483, 86-92 (2017-01-04)

When polysaccharide-based chiral columns are used in combination with aqueous-organic mobile phases for the separation of enantiomers in high-performance liquid chromatography the separation mode is commonly called "reversed-phase" in analogy to achiral separations. In several earlier and recent studies on

Global Trade Item Number

SKU	GTIN
233013-50G	04061831828931