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45393

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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Ona Sakaliene et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 44(1), 1-6 (2008-12-18)
Chlorpropham (isopropyl 3-chlorocarbanilate) is a pesticide used to control sprouting of potatoes during long-term storage. The objective of the present study was to establish the total chlorpropham residue balance (residues in unwashed and washed whole tubers, peeled tubers, peels, boiled
Y Nakagawa et al.
Xenobiotica; the fate of foreign compounds in biological systems, 34(3), 257-272 (2004-06-19)
1: The metabolism and action of chlorpropham (isopropyl N-(3-chlorophenyl)carbamate; CIPC, a post-harvest agent) were studied in freshly isolated rat hepatocytes, and the oestrogen-like activity of CIPC and its metabolites was assessed by in vitro assays. The exposure of hepatocyte suspensions
Junichi Eto et al.
FEBS letters, 550(1-3), 179-184 (2003-08-26)
An anti-chlorpropham single-chain variable-fragment (scFv) gene was introduced into Arabidopsis in a manner to express the antibody fragment in each of four different subcellular compartments. The accumulation of scFv in transgenic plants was detected by targeting the fragment in the
Xia Ge et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 81(1), 397-403 (2011-07-16)
An inclusion complex between the agrochemical chloropropham (CIPC) and β-cyclodextrin (β-CD) was prepared. A 2:1 host-guest stoichiometry was conformed by elemental analysis. From the phase solubility studies, the calculated stepwise stability constants were K(1)=224.6L/mol and K(2)=939.2L/mol, respectively. FT-IR, thermoanalysis and
Margaret J Smith et al.
Journal of hazardous materials, 246-247, 154-162 (2013-01-09)
DFT calculations were performed on the thermal reactions of chlorpropham 1, a carbamate pesticide and plant growth regulator frequently used in the storage of potatoes. At the conditions normally used in applying 1 (injection of a methanolic solution of 1
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