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Details

Stereochemistry ACHIRAL
Molecular Formula C12H16ClN4S
Molecular Weight 283.8
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of BECLOTIAMINE ION

SMILES

CC1=C(CCCl)SC=[N+]1CC2=C(N)N=C(C)N=C2

InChI

InChIKey=QNJSQRKKBAWIPT-UHFFFAOYSA-N
InChI=1S/C12H16ClN4S/c1-8-11(3-4-13)18-7-17(8)6-10-5-15-9(2)16-12(10)14/h5,7H,3-4,6H2,1-2H3,(H2,14,15,16)/q+1

HIDE SMILES / InChI
Beclotiamine (or chloroethyl thiamine) had been studied for veterinary and showed anticoccidial activity against Eimeria tenella, although metabolites and related substances were inactive. Information about the nowadays application of this compound is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Rapid and sensitive determination of amprolium in chicken plasma by high-performance liquid chromatography with post-column reaction.
1997-06-06
Studies on the mode of action of beclotiamine on Eimeria tenella.
1978-10
[Effect of beclotiamine on the thiamine requirements of Eimeria tenella and Eimeria acervulina].
1972-06
Patents
Name Type Language
BECLOTIAMINE ION
Common Name English
CHLOROTHIAMINE ION
Preferred Name English
3-((4-AMINO-2-METHYLPYRIMIDIN-5-YL)METHYL)-5-(2-CHLOROETHYL)-4-METHYL-1,3-THIAZOL-3-IUM
Systematic Name English
THIAMINE NITRATE IMPURITY C [EP IMPURITY]
Common Name English
3-((4-AMINO-2-METHYL-5-PYRIMIDINYL)METHYL)-5-(2-CHLOROETHYL)-4-METHYLTHIAZOLIUM
Systematic Name English
CHLOROTHIAMINE [EP IMPURITY]
Common Name English
THIAMINE HYDROCHLORIDE IMPURITY C [EP IMPURITY]
Common Name English
THIAZOLIUM, 3-((4-AMINO-2-METHYL-5-PYRIMIDINYL)METHYL)-5-(2-CHLOROETHYL)-4-METHYL-
Systematic Name English
Code System Code Type Description
FDA UNII
4W25FR6CGB
Created by admin on Tue Apr 01 23:58:23 GMT 2025 , Edited by admin on Tue Apr 01 23:58:23 GMT 2025
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PUBCHEM
71859
Created by admin on Tue Apr 01 23:58:23 GMT 2025 , Edited by admin on Tue Apr 01 23:58:23 GMT 2025
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CAS
20166-17-0
Created by admin on Tue Apr 01 23:58:23 GMT 2025 , Edited by admin on Tue Apr 01 23:58:23 GMT 2025
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