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Merck
CN

32086

Crufomate

PESTANAL®, analytical standard

别名:

(RS)-4-tert-Butyl-2-chlorophenyl methyl methylphosphoramidate, Amidofos, Amidophos, NSC 253463, Ruelene

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关于此项目

经验公式(希尔记法):
C12H19ClNO3P
化学文摘社编号:
分子量:
291.71
EC Number:
206-083-1
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
2133258
MDL number:
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InChI key

BOFHKBLZOYVHSI-UHFFFAOYSA-N

InChI

1S/C12H19ClNO3P/c1-12(2,3)9-6-7-11(10(13)8-9)17-18(15,14-4)16-5/h6-8H,1-5H3,(H,14,15)

SMILES string

CNP(=O)(OC)Oc1ccc(cc1Cl)C(C)(C)C

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

农药列管产品
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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D L Lewis et al.
Nature, 401(6756), 898-901 (1999-11-30)
Numerous anthropogenic chemicals of environmental concern--including some phenoxy acid herbicides, organophosphorus insecticides, polychlorinated biphenyls, phthalates, freon substitutes and some DDT derivatives--are chiral. Their potential biological effects, such as toxicity, mutagenicity, carcinogenicity, and endocrine disrupter activity, are generally enantiomer-selective, and different
Arthur W Garrison et al.
Methods in molecular biology (Clifton, N.J.), 384, 157-170 (2008-04-09)
The generic method described here involves typical capillary electrophoresis (CE) techniques, with the addition of cyclodextrin chiral selectors to the electrolyte for enantiomer separation and also, in the case of neutral analytes, the further addition of a micelle-forming compound such

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