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Details

Stereochemistry ACHIRAL
Molecular Formula C7H5N5O8
Molecular Weight 287.1433
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NITRAMINE

SMILES

CN(C1=C(C=C(C=C1[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O

InChI

InChIKey=AGUIVNYEYSCPNI-UHFFFAOYSA-N
InChI=1S/C7H5N5O8/c1-8(12(19)20)7-5(10(15)16)2-4(9(13)14)3-6(7)11(17)18/h2-3H,1H3

HIDE SMILES / InChI

Molecular Formula C7H5N5O8
Molecular Weight 287.1433
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Quantitative structure-activity relationships in two-electron reduction of nitroaromatic compounds by Enterobacter cloacae NAD(P)H:nitroreductase.
2001 Jan 1
Use of a Salmonella microsuspension bioassay to detect the mutagenicity of munitions compounds at low concentrations.
2001 Jan 25
Retro-nitroreductase, a putative evolutionary precursor to Enterobacter cloacae strain 96-3 nitroreductase.
2001 Oct
Development of marine toxicity data for ordnance compounds.
2001 Oct
Quantitative structure-activity relationships in enzymatic single-electron reduction of nitroaromatic explosives: implications for their cytotoxicity.
2001 Sep 3
Toxicological and chemical assessment of ordinance compounds in marine sediments and porewaters.
2002 Aug
Percutaneous absorption of explosives and related compounds: an empirical model of bioavailability of organic nitro compounds from soil.
2002 Jul 15
Oxidation of explosives by Fenton and photo-Fenton processes.
2003 Jul
Bioslurry treatment for soils contaminated with very high concentrations of 2,4,6-trinitrophenylmethylnitramine (tetryl).
2003 Jun 27
Tissue distribution and elimination of N-methyl-N-2,4,6-tetranitroaniline (tetryl) in rats.
2007 Dec
Relationship between mutagenicity and reactivity or biodegradability for nitroaromatic compounds.
2007 Feb
Metabolism, tissue distribution, and pharmacokinetics of N-methyl-N-2,4,6-tetranitroaniline (tetryl).
2007 Nov
Selective detection of trace nitroaromatic, nitramine, and nitrate ester explosive residues using a three-step fluorimetric sensing process: a tandem turn-off, turn-on sensor.
2007 Nov
Heats of sublimation of nitramines based on simple parameters.
2008 Apr 15
A review on slurry bioreactors for bioremediation of soils and sediments.
2008 Feb 29
Cytotoxicity of nitroaromatic explosives and their biodegradation products in mice splenocytes: implications for their immunotoxicity.
2008 Jul-Aug
A structural modelling study on marine sediments toxicity.
2008 Jun 26
Performance evaluation of a miniature ion mobility spectrometer drift cell for application in hand-held explosives detection ion mobility spectrometers.
2009 Sep
Detection of explosives as negative ions directly from surfaces using a miniature mass spectrometer.
2010 Jun 15
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:50:58 UTC 2023
Edited
by admin
on Fri Dec 15 17:50:58 UTC 2023
Record UNII
GJ18911991
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NITRAMINE
MI  
Common Name English
NITRAMINE [MI]
Common Name English
PICRYLMETHYLNITRAMINE
Common Name English
TETRYL
HSDB  
Common Name English
N-METHYL-N,2,4,6-TETRANITROBENZENAMINE
Systematic Name English
TETRALITE
Common Name English
TETRYL [HSDB]
Common Name English
NSC-2166
Code English
PICRYLNITROMETHYLAMINE
Systematic Name English
Code System Code Type Description
CHEBI
28950
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
WIKIPEDIA
TETRYL
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
MESH
C015384
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
NSC
2166
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
CHEBI
7579
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
EPA CompTox
DTXSID7047770
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
HSDB
2857
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
CAS
479-45-8
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
MERCK INDEX
m7929
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
207-531-9
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
FDA UNII
GJ18911991
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY
PUBCHEM
10178
Created by admin on Fri Dec 15 17:50:58 UTC 2023 , Edited by admin on Fri Dec 15 17:50:58 UTC 2023
PRIMARY