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CAMBENDAZOL

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CAMBENDAZOL Basic information

Product Name:
CAMBENDAZOL
Synonyms:
  • NSC377071;NOVAZOLE;MK 905;NOVIBEN;BONLAM
  • CS-2326
  • Cambenzide
  • Gamvet
  • N-[2-(4-Thiazolyl)-1H-benzimidazol-5-yl]carbamic acid 1-methylethyl ester
  • 2-(4-Thiazolyl)-5-isopropoxycarbonylaminobenzimidazole
  • NSC 377071
  • isopropyl 2-(thiazol-4-yl)-3H-benzo[d]imidazol-5-ylcarbamate
CAS:
26097-80-3
MF:
C14H14N4O2S
MW:
302.35
EINECS:
247-459-5
Mol File:
26097-80-3.mol
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CAMBENDAZOL Chemical Properties

Melting point:
212-214℃ (ethyl acetate hexane )
Density 
1.2909 (rough estimate)
refractive index 
1.6440 (estimate)
storage temp. 
Store at -20°C
solubility 
DMF: 10 mg/ml; DMSO: 10 mg/ml
pka
9.99±0.10(Predicted)
form 
Solid
color 
Light yellow to brown
BRN 
563292
Major Application
forensics and toxicology
pharmaceutical (small molecule)
InChI
1S/C14H14N4O2S/c1-8(2)20-14(19)16-9-3-4-10-11(5-9)18-13(17-10)12-6-21-7-15-12/h3-8H,1-2H3,(H,16,19)(H,17,18)
InChIKey
QZWHWHNCPFEXLL-UHFFFAOYSA-N
SMILES
CC(C)OC(=O)Nc1ccc2[nH]c(nc2c1)-c3cscn3
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Safety Information

Hazard Codes 
Xn
Risk Statements 
63
Safety Statements 
36/37
WGK Germany 
3
RTECS 
DD6538000
Storage Class
11 - Combustible Solids
Hazard Classifications
Repr. 2
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CAMBENDAZOL Usage And Synthesis

Description

Cambendazol is an antihelmintic that, at a dose of 50 mg/kg/day in mice, eradicates S. ratti adult worms from intestine and S. stercoralis larva from muscle. It inhibits polymerization of microtubules isolated from bovine brain with an IC50 value of 64.2 μM. Formulations containing cambendazol have been used to treat strongyloidiasis in humans and have been studied as potential chemotherapeutics.

Uses

Anthelmintic.

brand name

Camdan (Merck);.

References

[1] GROVE D I. Strongyloides ratti and S. stercoralis: the effects of thiabendazole, mebendazole, and cambendazole in infected mice.[J]. The American journal of tropical medicine and hygiene, 1982: 469-476. DOI: 10.4269/ajtmh.1982.31.469
[2] PAUL A. FRIEDMAN  Edward G P. Interaction of anthelmintic benzimidazoles and benzimidazole derivatives with bovine brain tubulin[J]. Biochimica et biophysica acta. General subjects, 1978, 544 3: Pages 605-614. DOI: 10.1016/0304-4165(78)90334-3
[3] S A BICALHO  Q P  O J Le?o. Cambendazole in the treatment of human strongyloidiasis.[J]. American Journal of Tropical Medicine and Hygiene, 1983, 32 5: 1181-1183. DOI: 10.4269/ajtmh.1983.32.1181
[4] ROSSE* G. Compositions and Methods for the Treatment of Mitochondrial Diseases[J]. ACS Medicinal Chemistry Letters, 2012, 3 12: 954. DOI: 10.1021/ml3002924

CAMBENDAZOLSupplier

Shanghai Boyle Chemical Co., Ltd.
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Email
sales@boylechem.com
J & K SCIENTIFIC LTD.
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18210857532; 18210857532
Email
jkinfo@jkchemical.com
AdooQ BioScience, LLC
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+1 (866) 930-6790
Email
info@adooq.com
Bide Pharmatech Ltd.
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400-400-164-7117 18317119277
Email
product02@bidepharm.com
Quality Control Solutions Ltd.
Tel
66853366 13670046396
Email
sales@chem-strong.com
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