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Merck
CN

PS355

毒草胺

analytical standard

别名:

2-氯-N-异丙基乙酰苯胺

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关于此项目

经验公式(希尔记法):
C11H14ClNO
化学文摘社编号:
分子量:
211.69
EC Number:
217-638-2
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
2103903
MDL number:
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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

SMILES string

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

InChI

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

InChI key

MFOUDYKPLGXPGO-UHFFFAOYSA-N

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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

signalword

Danger

Hazard Classifications

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

存储类别

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

法规信息

农药列管产品
危险化学品

此项目有


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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
A R Loch et al.
Environmental science & technology, 36(19), 4065-4073 (2002-10-17)
Reactions of bisulfide and polysulfides with alachlor, propachlor, and metolachlor were examined in aqueous solution to investigate the role reduced sulfur species could play in effecting abiotic transformations of chloroacetanilide herbicides. Experiments at 25 degrees C demonstrated that reactions were

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