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Merck
CN

PS355

Propachlor

analytical standard

Synonym(s):

2-Chloro-N-isopropylacetanilide

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About This Item

Empirical Formula (Hill Notation):
C11H14ClNO
CAS Number:
1918-16-7
Molecular Weight:
211.69
EC Number:
217-638-2
UNSPSC Code:
41116107
PubChem Substance ID:
24899193
Beilstein/REAXYS Number:
2103903
MDL number:
MFCD00078731

Key Documents

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SMILES string

CC(C)N(C(=O)CCl)c1ccccc1

InChI key

MFOUDYKPLGXPGO-UHFFFAOYSA-N

InChI

1S/C11H14ClNO/c1-9(2)13(11(14)8-12)10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3

grade

analytical standard

packaging

ampule of 250 mg

manufacturer/tradename

Chem Service, Inc. PS-355

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
environmental

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.

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

农药列管产品
危险化学品
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Ioannis K Konstantinou et al.
Water research, 36(11), 2733-2742 (2002-07-31)
The light-induced degradation of propachlor (2-chloro-N-isopropylacetanilide) under simulated solar irradiation has been investigated in aqueous solutions containing TiO2 suspensions as photocatalysts. The study focuses on the identification of possible intermediate products and the determination of inorganic ions formed during the
Katrice A Lippa et al.
Environmental toxicology and chemistry, 24(10), 2401-2409 (2005-11-05)
Second-order rate constants (kNuc) for aqueous-phase bimolecular nucleophilic substitution (SN2) reactions of a range of anionic nucleophiles with alachlor, propachlor, and two analogs of propachlor (a thioacetanilide and a beta-anilide) were fit to the Swain-Scott and Edwards models. Correlations of
C S Liu et al.
Chemosphere, 85(9), 1438-1443 (2011-09-07)
Chloroacetanilide herbicides are extensively used in the control of weeds and have widely resulted in nonpoint contamination of groundwater and soil resources. In the attempt to achieve better remediation for herbicide-contaminated resources, we investigated the reductive transformation of propachlor through
P J Dierickx
Cell biology and toxicology, 15(5), 325-332 (2000-05-17)
Alachlor, metolachlor, and propachlor are widely used chloroacetanilide herbicides. Their cytotoxicity in rat (Fa32) and human (Hep G2) hepatoma-derived cells was investigated, in connection with their influence on the endogenous glutathione (GSH) content, on the xenobiotic-metabolizing phase I enzymes 7-ethoxyresorufin
Wei Zheng et al.
Environmental science & technology, 38(24), 6855-6860 (2005-01-27)
Propachlor and other chloroacetanilide herbicides are frequently detected contaminants of groundwater and surface water in agricultural regions. The purpose of this work was to develop a new approach to remove propachlor residues from the environment via chemical remediation by the
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