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Details

Stereochemistry ACHIRAL
Molecular Formula C6H4N2O5
Molecular Weight 184.1064
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,4-DINITROPHENOL

SMILES

OC1=CC=C(C=C1[N+]([O-])=O)[N+]([O-])=O

InChI

InChIKey=UFBJCMHMOXMLKC-UHFFFAOYSA-N
InChI=1S/C6H4N2O5/c9-6-2-1-4(7(10)11)3-5(6)8(12)13/h1-3,9H

HIDE SMILES / InChI

Molecular Formula C6H4N2O5
Molecular Weight 184.1064
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 15:10:50 UTC 2023
Edited
by admin
on Fri Dec 15 15:10:50 UTC 2023
Record UNII
Q13SKS21MN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,4-DINITROPHENOL
HSDB   MI  
Systematic Name English
.ALPHA.-DINITROPHENOL
Common Name English
ALDIFEN
Brand Name English
PHENOL, 2,4-DINITRO-
Systematic Name English
DINITROPHENOL [MART.]
Common Name English
NSC-1532
Code English
NITROPHENE
Brand Name English
MP-101
Code English
DINITROPHENOL
MART.   WHO-DD  
Systematic Name English
2,4-DINITROPHENOL [HSDB]
Common Name English
1,3-DINITRO-4-HYDROXYBENZENE
Systematic Name English
NITROPHEN
Brand Name English
MITCAL
Brand Name English
Dinitrophenol [WHO-DD]
Common Name English
FENOXYL CARBON N
Brand Name English
CHEMOX
Common Name English
2,4-DINITROPHENOL [MI]
Common Name English
1-HYDROXY-2,4-DINITROBENZENE
Systematic Name English
DINOFAN
Brand Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 764820
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
EPA PESTICIDE CODE 37509
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
FDA ORPHAN DRUG 672818
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
Code System Code Type Description
CHEBI
84561
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
CHEBI
42017
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
CHEBI
39352
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
PUBCHEM
1493
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
NSC
1532
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
FDA UNII
Q13SKS21MN
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
MERCK INDEX
m4578
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY Merck Index
DRUG BANK
DB04528
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
HSDB
529
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
WIKIPEDIA
2,4-DINITROPHENOL
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
EVMPD
SUB33423
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
CAS
51-28-5
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
SMS_ID
100000126132
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
EPA CompTox
DTXSID0020523
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-087-7
Created by admin on Fri Dec 15 15:10:50 UTC 2023 , Edited by admin on Fri Dec 15 15:10:50 UTC 2023
PRIMARY
Related Record Type Details
TARGET->INHIBITOR OF EXPRESSION
DNP decreases the formation of high-energy phosphate bonds in mitochondria and at the same time stimulates systemic oxygen consumption. This dissociative effect is known as uncoupling of oxidative phosphorylation. Weak uncoupler.
SALT/SOLVATE -> PARENT
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ACTIVE MOIETY