Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Analytical Chemistry >  Standard >  Veterinary drug and Pesticide residues >  2,6-Dichlorothiobenzamide

2,6-Dichlorothiobenzamide

Basic information Safety Supplier Related

2,6-Dichlorothiobenzamide Basic information

Product Name:
2,6-Dichlorothiobenzamide
Synonyms:
  • chlorthiamide
  • chlorthioamide
  • chlortiamid
  • dcbn
  • prefix
  • sd7961
  • CHLORTHIAMID PESTANAL (2,6-DICHLORO-THIO
  • Prefix[R]
CAS:
1918-13-4
MF:
C7H5Cl2NS
MW:
206.09
EINECS:
217-637-7
Mol File:
1918-13-4.mol
More
Less

2,6-Dichlorothiobenzamide Chemical Properties

Melting point:
151-152°C
Boiling point:
320.6±52.0 °C(Predicted)
Density 
1.4704 (rough estimate)
refractive index 
1.6300 (estimate)
Flash point:
>100 °C
storage temp. 
-20°C Freezer, Under inert atmosphere
solubility 
DMSO (Slightly), Methanol (Slightly)
pka
11.71±0.29(Predicted)
color 
White to Pale Beige
Water Solubility 
0.95g/L(21 ºC)
BRN 
1910353
CAS DataBase Reference
1918-13-4(CAS DataBase Reference)
EPA Substance Registry System
Chlorthiamid (1918-13-4)
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
36
WGK Germany 
1
RTECS 
CV3850000
Hazard Note 
Harmful
HazardClass 
IRRITANT
HS Code 
2930909899
Toxicity
LD50 oral in rabbit: 300mg/kg

MSDS

  • Language:English Provider:ACROS
More
Less

2,6-Dichlorothiobenzamide Usage And Synthesis

Definition

ChEBI: 2,6-dichlorothiobenzamide is a dichlorobenzene and a thiocarboxamide. It has a role as a proherbicide and an agrochemical.

Safety Profile

Poison by ingestion and intraperitoneal route. Moderately toxic by skin contact. Mutation data reported. An herbicide. When heated to decomposition it emits very toxic fumes of Cl-, NOx, and sox.

Metabolic pathway

Twelve metabolites are isolated from either urine or bile from either rats (11 metabolites) or goats (seven metabolites) given single oral doses of 14C-labeled 2,6-dichlorobenzonitrile (DCBN). Five of these metabolites are also excreted in urine from rats dosed orally with 2,6-dichlorothiobenzamide (DCTBA) which is an acid amide analog. All metabolites from either DCBN or DCTBA are benzonitriles with the following ring substituents: Cl2, OH (three isomers); Cl2, (OH)2; Cl, (OH)2; Cl, OH, SH; Cl, OH, SCH3; SOCH3, OH; Cl2, S-(N-acetyl)cysteine; Cl, S-(N-acetyl)cysteine; Cl, OH, S-(N-acetyl)cysteine.
The thiobenzamide moiety of DCTBA is converted to the nitrile in all extracted urinary metabolites. No hydrolysis of the nitrile in DCBN to either amide or an acid is detected. Urine is the major route for excretion; however, enterohepatic circulation occurs.

2,6-DichlorothiobenzamideSupplier

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Email
market03@meryer.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com