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Details

Stereochemistry ACHIRAL
Molecular Formula C15H24O
Molecular Weight 220.3505
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTYLATED HYDROXYTOLUENE

SMILES

CC1=CC(=C(O)C(=C1)C(C)(C)C)C(C)(C)C

InChI

InChIKey=NLZUEZXRPGMBCV-UHFFFAOYSA-N
InChI=1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3

HIDE SMILES / InChI

Molecular Formula C15H24O
Molecular Weight 220.3505
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:08:02 UTC 2023
Edited
by admin
on Fri Dec 15 15:08:02 UTC 2023
Record UNII
1P9D0Z171K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTYLATED HYDROXYTOLUENE
FHFI   HSDB   II   MART.   MI   NF   USP-RS   VANDF   WHO-DD   WHO-IP  
Common Name English
Butylated hydroxytoluene [WHO-DD]
Common Name English
BUTYLATED HYDROXYTOLUENE [USP-RS]
Common Name English
INS NO.321
Code English
BUTYLATED HYDROXYTOLUENE [II]
Common Name English
BUTYLHYDROXYTOLUENE [EP MONOGRAPH]
Common Name English
E-321
Code English
PHENOL, 2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYL-
Systematic Name English
BUTYLATED HYDROXYTOLUENE [VANDF]
Common Name English
BUTYLATED HYDROXYTOLUENE (E 321)
Common Name English
BUTYLATED HYDROXYTOLUENE [FHFI]
Common Name English
BUTYLHYDROXYTOLUENE
EP  
Systematic Name English
2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYLPHENOL
Systematic Name English
BUTYLATED HYDROXYTOLUENE [IARC]
Common Name English
BUTYLATED HYDROXYTOLUENE [MART.]
Common Name English
BHT [FCC]
Common Name English
2,6-DI-TERT-BUTYL-P-CRESOL
Common Name English
KERABIT
Common Name English
BUTYLATED HYDROXYTOLUENE [NF]
Common Name English
4-METHYL-2,6-DITERTIARY-BUTYL-PHENOL
Common Name English
2,6-DI-TERT-BUTYL-P-CRESOL2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYL-PHENOL
Systematic Name English
NSC-6347
Code English
BUTYLATED HYDROXYTOLUENE [HSDB]
Common Name English
FEMA NO. 2184
Code English
BHT
FCC   INCI  
INCI  
Official Name English
BUTYLATED HYDROXYTOLUENE [MI]
Common Name English
INS-321
Code English
2,6-DITERTIARY-BUTYL-P-CRESOL
Common Name English
BUTYLATED HYDROXYTOLUENE [WHO-IP]
Common Name English
BHT [INCI]
Common Name English
BUTYLHYDROXYTOLUENUM [WHO-IP LATIN]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 22105
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
JECFA EVALUATION INS-321
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
CODEX ALIMENTARIUS (GSFA) INS-321
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
NCI_THESAURUS C275
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
CFR 21 CFR 172.115
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
Code System Code Type Description
CHEBI
34247
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
MERCK INDEX
m2820
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY Merck Index
SMS_ID
100000076384
Created by admin on Fri Dec 15 15:08:03 UTC 2023 , Edited by admin on Fri Dec 15 15:08:03 UTC 2023
PRIMARY
ChEMBL
CHEMBL146
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
NSC
6347
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
MESH
D002084
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
EVMPD
SUB11765MIG
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
RS_ITEM_NUM
1082708
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
NCI_THESAURUS
C322
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
DAILYMED
1P9D0Z171K
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
FDA UNII
1P9D0Z171K
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
CAS
128-37-0
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
ECHA (EC/EINECS)
204-881-4
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
EPA CompTox
DTXSID2020216
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
WIKIPEDIA
BUTYLATED HYDROXYTOLUENE
Created by admin on Fri Dec 15 15:08:03 UTC 2023 , Edited by admin on Fri Dec 15 15:08:03 UTC 2023
PRIMARY
RXCUI
1848
Created by admin on Fri Dec 15 15:08:03 UTC 2023 , Edited by admin on Fri Dec 15 15:08:03 UTC 2023
PRIMARY RxNorm
HSDB
1147
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
PUBCHEM
31404
Created by admin on Fri Dec 15 15:08:02 UTC 2023 , Edited by admin on Fri Dec 15 15:08:02 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
BUTYLATED HYDROXYTOLUENE
Created by admin on Fri Dec 15 15:08:03 UTC 2023 , Edited by admin on Fri Dec 15 15:08:03 UTC 2023
PRIMARY Description: Colourless crystals or a white or almost white, crystalline powder; odour, faint and characteristic. Solubility: Practically insoluble in water; freely soluble in ethanol (~750 g/l) TS, acetone R, ether R, and arachis oil R. Category: Antioxidant. Storage: Butylated hydroxytoluene should be kept in a well-closed container, protected from light.
Related Record Type Details
METABOLITE -> PARENT
METABOLITE -> PARENT
MAJOR
Related Record Type Details
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
IMPURITY -> PARENT
Related Record Type Details
ACTIVE MOIETY
http://apps.who.int/phint/pdf/b/Jb.6.1.65.pdf