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About This Item
Linear Formula:
C10H12NO2Cl
CAS Number:
Molecular Weight:
213.66
Beilstein/REAXYS Number:
2211397
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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assay
~95%
form
crystalline
color
light tan
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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Biochem/physiol Actions
A mitotic poison; inhibits plant metabolism.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 2 - STOT RE 2
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
T Fujitani et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 39(3), 253-259 (2001-03-30)
Male F344 rats were given 0 or 3% chlorpropham in the diet and at 2, 4, 6, 8 or 13 weeks of administration, five rats in each group were examined for hematology, plasma clinical chemistry and pathology. Marked splenomegaly 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
Margaret J Smith et al.
Environment international, 49, 38-50 (2012-09-18)
Chlorpropham (CIPC) was introduced in 1951 and is a primary N-phenyl carbamate belonging to a group of pesticides known as carbamates which are estimated to account for 11% of the total insecticide sales worldwide. They were considered less toxic than
Haya Friedman et al.
Planta, 216(6), 1034-1042 (2003-04-11)
The involvement of the actin and the microtubule cytoskeleton networks in the gravitropic response of snapdragon ( Antirrhinum majus L.) flowering shoots was studied using various specific cytoskeleton modulators. The microtubule-depolymerizing drugs tested had no effect on gravitropic bending. In
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