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32086

Supelco

Crufomate

PESTANAL®, analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C12H19ClNO3P
CAS Number:
299-86-5
Molecular Weight:
291.71
Beilstein/REAXYS Number:
2133258
EC Number:
206-083-1
MDL number:
MFCD00055452
UNSPSC Code:
41116107
PubChem Substance ID:
329753730

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

SMILES string

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

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)

InChI key

BOFHKBLZOYVHSI-UHFFFAOYSA-N

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
GHS07,GHS09

signalword

Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

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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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