NITRAMINE

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 Search

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

Title	Date	PubMed
Detection of explosives as negative ions directly from surfaces using a miniature mass spectrometer.	2010-06-15	20496904
Performance evaluation of a miniature ion mobility spectrometer drift cell for application in hand-held explosives detection ion mobility spectrometers.	2009-09	19424683
Cytotoxicity of nitroaromatic explosives and their biodegradation products in mice splenocytes: implications for their immunotoxicity.	2008-09-25	18810995
A structural modelling study on marine sediments toxicity.	2008-06-26	18728732
Heats of sublimation of nitramines based on simple parameters.	2008-04-15	17765395
A review on slurry bioreactors for bioremediation of soils and sediments.	2008-02-29	18312630
Tissue distribution and elimination of N-methyl-N-2,4,6-tetranitroaniline (tetryl) in rats.	2007-12	17680234
Metabolism, tissue distribution, and pharmacokinetics of N-methyl-N-2,4,6-tetranitroaniline (tetryl).	2007-11	21783812
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.	2007-11	17944906
Relationship between mutagenicity and reactivity or biodegradability for nitroaromatic compounds.	2007-02	17713210
Oxidation of explosives by Fenton and photo-Fenton processes.	2003-07	14509704
Bioslurry treatment for soils contaminated with very high concentrations of 2,4,6-trinitrophenylmethylnitramine (tetryl).	2003-06-27	12835026
Toxicological and chemical assessment of ordinance compounds in marine sediments and porewaters.	2002-08	12269482
Percutaneous absorption of explosives and related compounds: an empirical model of bioavailability of organic nitro compounds from soil.	2002-07-15	12140179
Retro-nitroreductase, a putative evolutionary precursor to Enterobacter cloacae strain 96-3 nitroreductase.	2001-10	11761325
Development of marine toxicity data for ordnance compounds.	2001-10	11503067
Quantitative structure-activity relationships in enzymatic single-electron reduction of nitroaromatic explosives: implications for their cytotoxicity.	2001-09-03	11514095
Use of a Salmonella microsuspension bioassay to detect the mutagenicity of munitions compounds at low concentrations.	2001-01-25	11152971
Quantitative structure-activity relationships in two-electron reduction of nitroaromatic compounds by Enterobacter cloacae NAD(P)H:nitroreductase.	2001-01-01	11361014

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:55:14 GMT 2025` Edited by `admin` on `Mon Mar 31 18:55:14 GMT 2025`
Record UNII	GJ18911991
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

TETRYL

Preferred Name

English

NITRAMINE

Common Name

English

NITRAMINE [MI]

Common Name

English

PICRYLMETHYLNITRAMINE

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