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Supelco

Chlorpropham

PESTANAL®, analytical standard

Synonym(s):

Chloro-ICP, Chloropropham, Isopropyl N-(3-chlorophenyl)carbamate

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About This Item

Linear Formula:
C10H12NO2Cl
CAS Number:
101-21-3
Molecular Weight:
213.66
Beilstein:
2211397
EC Number:
202-925-7
MDL number:
MFCD00037108
UNSPSC Code:
41116107
PubChem Substance ID:
329756697
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

CC(C)OC(=O)Nc1cccc(Cl)c1

InChI

1S/C10H12ClNO2/c1-7(2)14-10(13)12-9-5-3-4-8(11)6-9/h3-7H,1-2H3,(H,12,13)

InChI key

CWJSHJJYOPWUGX-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.

Legal Information

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

Signal Word

Warning

Hazard Statements

H302,H351,H373,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - STOT RE 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ9071
BCBZ3405
BCBV7468
SZBC293XV
SZB8315XV

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Helen Ferrier et al.
Food additives and contaminants, 23(6), 601-615 (2006-06-13)
The assessment of consumer exposure to pesticides is an important part of pesticide regulation. Probabilistic modelling allows analysis of uncertainty and variability in risk assessments. The output of any assessment will be influenced by the characteristics and uncertainty of the
Dong-xian Liu et al.
Fa yi xue za zhi, 23(4), 292-294 (2007-09-28)
The extraction method for separating buprenorphine from urine was described. Buprenorphine was extracted with chloroform at pH7 or with SPE (extracted by organic support 401 at pH10.8, then eluted with chloroform), finally determined by GC-NPD. The extracted yields of the
S Noël et al.
Mededelingen (Rijksuniversiteit te Gent. Fakulteit van de Landbouwkundige en Toegepaste Biologische Wetenschappen), 67(3), 431-439 (2003-04-17)
Studies carried out in 1999 by the University of Ghent showed that 36% of potatoes' samples contained Chlorprophame (CIPC) residues and that 7.9% of them exceeded the maximal limit of residues (RML), fixed at 5 ppm. The heterogeneity of sprout
T Fujitani et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 38(7), 617-625 (2000-08-15)
Male and female ICR mice were given 0, 1875, 7500 or 30,000 ppm of chlorpropham (CIPC) in the diet for 13 weeks. Methemoglobin levels of male and female mice in the 7500 and 30,000 ppm groups were significantly elevated. Hemoglobin
Yoshio Nakagawa et al.
Toxicology, 200(2-3), 123-133 (2004-06-24)
The metabolism and action of chlorpropham (isopropyl N-(3-chlorophenyl)carbamate; CIPC, a post-harvest agent) and its metabolites were studied in freshly isolated rat hepatocytes and isolated rat hepatic mitochondria, respectively. The exposure of hepatocytes to CIPC caused a concentration (0.25-1.0 mM)- and
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Protocols

US EPA Method 632: HPLC Analysis of Pesticides on Ascentis® C18

-methylcarbamate 10 μg/mL; Diuron; Propham; Siduron; Methiocarb, analytical standard; Linuron 10 μg/mL; Swep 10 μg/mL; Chlorpropham 10 μg/mL; Barban; Neburon

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