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111988-49-9

111988-49-9 structural image
Product Name: Thiacloprid
Formula: C10H9ClN4S
Synonyms: [3-(6-Chloro-3-pyridinylmethyl)-2-thiazolidinylidene]cyanamide
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CHEMICAL AND PHYSICAL PROPERTIES

Physical Description Odorless solid; [HSDB]
Color/Form Yellowish crystalline powder
Odor Odorless
Boiling Point decomp >270 °C
Melting Point 136 °C
Solubility In water, 185 mg/L at 20 °C
Density 1.46 g at 20 °C
Vapor Pressure 6.0X10-12 mm Hg at 20 °C (23X10-12 hPa at 20 °C)
LogP log Kow = 1.26 at 20 °C
Stability/Shelf Life Stable under recommended storage conditions.
Decomposition When heated to decomposition it emits toxic vapors of /nitrogen oxides, sulfur oxides, and chloride/.
pH pH = 7.4 at 20 °C
Collision Cross Section 154.84 Ų [M+H]+ [CCS Type: TW]
Other Experimental Properties Yellowish powder. Vapor pressure: 2.25X10-12 mm Hg (3X10-10 Pa) at 20 °C; solubility in water, 185 mg/L at 20 °C /Z-Thiacloprid/
Chemical Classes Pesticides -> Insecticides, Neonicotinoid

SAFETY INFORMATION

Signal word Danger
Pictogram(s)

Skull and Crossbones
Acute Toxicity
GHS06

Health Hazard
GHS08

Environment
GHS09
GHS Hazard Statements H301:Acute toxicity,oral
H332:Acute toxicity,inhalation
H336:Specific target organ toxicity,single exposure; Narcotic effects
H351:Carcinogenicity
H410:Hazardous to the aquatic environment, long-term hazard
Precautionary Statement Codes P201:Obtain special instructions before use.
P273:Avoid release to the environment.

COMPUTED DESCRIPTORS

Molecular Weight 252.72 g/mol
XLogP3 2.2
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 2
Exact Mass 252.0236452 g/mol
Monoisotopic Mass 252.0236452 g/mol
Topological Polar Surface Area 77.6 Ų
Heavy Atom Count 16
Formal Charge 0
Complexity 324
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

PRODUCT INTRODUCTION

description

Thiacloprid is a nitrile that is cyanamide in which the hydrogens are replaced by a 1,3-thiazolidin-2-ylidene group which in turn is substituted by a (6-chloropyridin-3-yl)methyl group at the ring nitrogen. It has a role as a xenobiotic, an environmental contaminant and a neonicotinoid insectide. It is a member of thiazolidines, a nitrile and a monochloropyridine. It is functionally related to a 2-chloropyridine and a cyanamide.