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Details

Stereochemistry ACHIRAL
Molecular Formula C10H7N3S
Molecular Weight 201.248
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of THIABENDAZOLE

SMILES

N1C2=CC=CC=C2N=C1C3=CSC=N3

InChI

InChIKey=WJCNZQLZVWNLKY-UHFFFAOYSA-N
InChI=1S/C10H7N3S/c1-2-4-8-7(3-1)12-10(13-8)9-5-14-6-11-9/h1-6H,(H,12,13)

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
THIABENDAZOLE
GREEN BOOK   HSDB   INCI   ISO   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF  
USAN   INCI  
Official Name English
THIABENDAZOLE [USP MONOGRAPH]
Common Name English
TIABENDAZOLE
EP   INN   JAN   MART.   WHO-DD   WHO-IP  
INN  
Official Name English
LOMBRISTOP
Common Name English
2-(4-Thiazolyl)benzimidazole
Systematic Name English
THIABENDAZOLE [INCI]
Common Name English
THIABENDAZOLE [USP-RS]
Common Name English
OMNIZOLE
Common Name English
2-(THIAZOL-4-YL)BENZIMIDAZOLE
Systematic Name English
MINZOLUM
Common Name English
Tiabendazole [WHO-DD]
Common Name English
1H-BENZIMIDAZOLE, 2-(4-THIAZOLYL)-
Systematic Name English
THIABENZOLE
Common Name English
THIABENDAZOLE [ORANGE BOOK]
Common Name English
NSC-525040
Code English
2-(4-THIAZOLYL)-1H-BENZIMIDAZOLE
Systematic Name English
TIABENDAZOLE [WHO-IP]
Common Name English
NEMAPAN
Common Name English
PITRIZET
Common Name English
THIABENDAZOLE [GREEN BOOK]
Common Name English
THIABENDAZOLE [USAN]
Common Name English
tiabendazole [INN]
Common Name English
TIABENDAZOLE [MART.]
Common Name English
THIABENDAZOLE [MI]
Common Name English
TIABENDAZOLE [JAN]
Common Name English
TIABENDAZOLE [EP MONOGRAPH]
Common Name English
THIABENDAZOLE [VANDF]
Common Name English
MK-360
Code English
THIABENDAZOLE [HSDB]
Common Name English
MINTEZOL
Brand Name English
TIABENDAZOLE [EP IMPURITY]
Common Name English
THIABENDAZOLE [ISO]
Common Name English
NSC-90507
Code English
Classification Tree Code System Code
WHO-ATC P02CA02
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 520.2380C
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 520.2380F
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
LIVERTOX NBK548194
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
WHO-ATC D01AC06
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
WHO-VATC QP52AC10
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 520.2380A
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 520.2380D
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 558.600
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
NDF-RT N0000175481
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
EPA PESTICIDE CODE 60101
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
WHO-VATC QD01AC06
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 520.2380E
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 520.2380B
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 520.2380
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 556.730
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
CFR 21 CFR 524.1484G
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
NCI_THESAURUS C250
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
Code System Code Type Description
ECHA (EC/EINECS)
205-725-8
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
RS_ITEM_NUM
1655000
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
INN
1436
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
NCI_THESAURUS
C873
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
THIABENDAZOLE
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY Description: A white to almost white powder; odourless or almost odourless. Solubility: Practically insoluble in water; soluble in 150 parts of ethanol (~750 g/l) TS; slightly soluble in ether R. Category: Anthelmintic. Storage: Tiabendazole should be kept in a well-closed container. Definition: Tiabendazole contains not less than 98.0% and not more than 101.0% of C10H7N3S, calculated with reference to the dried substance.
DAILYMED
N1Q45E87DT
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
EVMPD
SUB10996MIG
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
NSC
90507
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
NSC
525040
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
WIKIPEDIA
TIABENDAZOLE
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
MESH
D013827
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
SMS_ID
100000082153
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
FDA UNII
N1Q45E87DT
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
CHEBI
45979
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
ALANWOOD
thiabendazole
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
EPA CompTox
DTXSID0021337
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
MERCK INDEX
m10710
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL625
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
DRUG CENTRAL
2621
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
CAS
148-79-8
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
RXCUI
10450
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY RxNorm
IUPHAR
7304
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
HSDB
2027
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
PUBCHEM
5430
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
DRUG BANK
DB00730
Created by admin on Fri Dec 15 15:02:55 UTC 2023 , Edited by admin on Fri Dec 15 15:02:55 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of THIABENDAZOLE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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