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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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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

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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K L Davison et al.
Xenobiotica; the fate of foreign compounds in biological systems, 24(10), 1003-1012 (1994-10-01)
1. 14C-labelled propachlor, alachlor, butachlor, metolachlor, methoxypropachlor and some of their mercapturic acid pathway metabolites (MAP) were given to rat either by gavage or by perfusion into a renal artery. MAP metabolites were isolated from bile and urine. 2. Rat
Sheng Tai et al.
Molecular cancer therapeutics, 11(6), 1320-1331 (2012-04-12)
PI3K/AKT/mTOR pathway plays a key role in the tumorigenesis of many human cancers including prostate cancer. However, inhibitors of this pathway, such as Rad001, have not shown therapeutic efficacy as a single agent. Through a high-throughput screen of 5,000 widely
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
M B Genter et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 47(6), 1051-1057 (2009-05-09)
Alachlor and butachlor are chloracetanilide herbicides that induce olfactory tumors in rats, whereas propachlor does not. The mechanism by which alachlor induces tumors is distinct from many other nasal carcinogens, in that alachlor induces a gradual de-differentiation of the olfactory
Katrice A Lippa et al.
Journal of agricultural and food chemistry, 52(10), 3010-3021 (2004-05-13)
The ease with which alpha-chloroacetanilide herbicides undergo displacement reactions with strong nucleophiles, and their recalcitrance toward weak ones, is intimately related to their herbicidal properties and environmental chemistry. In this study, we investigate the kinetics and mechanisms of nucleophilic substitution

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