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Details

Stereochemistry ACHIRAL
Molecular Formula C5H7N3O3
Molecular Weight 157.1274
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-METHYL-5-NITRO-2-IMIDAZOLEMETHANOL

SMILES

CN1C(CO)=NC=C1[N+]([O-])=O

InChI

InChIKey=JSAQDPJIVQMBAY-UHFFFAOYSA-N
InChI=1S/C5H7N3O3/c1-7-4(3-9)6-2-5(7)8(10)11/h2,9H,3H2,1H3

HIDE SMILES / InChI

Molecular Formula C5H7N3O3
Molecular Weight 157.1274
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Determination of the persistence of dimetridazole, metronidazole and ronidazole residues in black tiger shrimp (Penaeus monodon) tissue and their stability during cooking.
2015
Ronidazole toxicosis in 3 society finches (Lonchura striata).
2010-03
Validated method for determination of eight banned nitroimidazole residues in natural casings by LC/MS/MS with solid-phase extraction.
2009-06-03
Validation of a liquid chromatography-tandem mass spectrometry method for the identification and quantification of 5-nitroimidazole drugs and their corresponding hydroxy metabolites in lyophilised pork meat.
2009-01-09
Simultaneous determination of nitroimidazole residues in honey samples by high-performance liquid chromatography with ultraviolet detection.
2007-06-22
Confirmation of four nitroimidazoles in porcine liver by liquid chromatography-tandem mass spectrometry.
2007-03-14
Determination of nitroimidazoles and their metabolites in swine tissues by liquid chromatography.
2003-07-11
Validation of a method for the detection and confirmation of nitroimidazoles and corresponding hydroxy metabolites in turkey and swine muscle by means of gas chromatography-negative ion chemical ionization mass spectrometry.
2001-09-15
The identification and assay of 2-methyl-5-nitroimidazole in pigs treated with dimetridazole.
1991-07-01
Dimetridazole residues in pork tissue. II. Application of liquid chromatographic method to monitor elimination of drug and its major metabolite.
1988-11-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:36:02 GMT 2025
Edited
by admin
on Mon Mar 31 21:36:02 GMT 2025
Record UNII
D4DG80JB2E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HYDROXYDIMETRIDAZOLE
Preferred Name English
1-METHYL-5-NITRO-2-IMIDAZOLEMETHANOL
Systematic Name English
IMIDAZOLE-2-METHANOL, 1-METHYL-5-NITRO-
Systematic Name English
2-HYDROXYMETHYL-1-METHYL-5-NITROIMIDAZOLE
Systematic Name English
1-METHYL-5-NITRO-1H-IMIDAZOLE-2-METHANOL
Systematic Name English
1-METHYL-2-HYDROXYMETHYL-5-NITROIMIDAZOLE
Systematic Name English
Code System Code Type Description
CAS
936-05-0
Created by admin on Mon Mar 31 21:36:02 GMT 2025 , Edited by admin on Mon Mar 31 21:36:02 GMT 2025
PRIMARY
FDA UNII
D4DG80JB2E
Created by admin on Mon Mar 31 21:36:02 GMT 2025 , Edited by admin on Mon Mar 31 21:36:02 GMT 2025
PRIMARY
MESH
C059098
Created by admin on Mon Mar 31 21:36:02 GMT 2025 , Edited by admin on Mon Mar 31 21:36:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
213-312-9
Created by admin on Mon Mar 31 21:36:02 GMT 2025 , Edited by admin on Mon Mar 31 21:36:02 GMT 2025
PRIMARY
PUBCHEM
557356
Created by admin on Mon Mar 31 21:36:02 GMT 2025 , Edited by admin on Mon Mar 31 21:36:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID30878799
Created by admin on Mon Mar 31 21:36:02 GMT 2025 , Edited by admin on Mon Mar 31 21:36:02 GMT 2025
PRIMARY