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RDX solution

1000 μg/mL in acetonitrile, ampule of 1.2 mL, certified reference material, Cerilliant®

Synonym(s):

Hexahydro-1,3,5-trinitro-1,3,5-triazine, Hexahydro-1,3,5-trinitro-1,3,5-triazine solution

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About This Item

Empirical Formula (Hill Notation):
C3H6N6O6
CAS Number:
121-82-4
Molecular Weight:
222.12
MDL number:
MFCD00458725
UNSPSC Code:
41116107
NACRES:
NA.24

grade

certified reference material

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1.2 mL

manufacturer/tradename

Cerilliant®

concentration

1000 μg/mL in acetonitrile

application(s)

environmental

format

single component solution

storage temp.

−20°C

SMILES string

O=[N+]([O-])N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1

InChI

1S/C3H6N6O6/c10-7(11)4-1-5(8(12)13)3-6(2-4)9(14)15/h1-3H2

InChI key

XTFIVUDBNACUBN-UHFFFAOYSA-N

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Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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J G Giarrizzo et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 925, 70-75 (2013-03-26)
A simple, fast liquid-liquid extraction method was developed for studying hexahydro-1,3,5-trinitro-1,3,5 triazine (RDX) biodegradation using small sample volumes. The method was tested in vitro with anaerobic incubations of RDX with whole rumen fluid (WRF) and a commercial Sporanaerobacter acetigenes strain
Karl J Indest et al.
Applied and environmental microbiology, 79(5), 1746-1750 (2013-01-01)
The transcriptome of RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine)-degrading strain Gordonia sp. strain KTR9 and its glnR mutant were studied as a function of nitrogen availability to further investigate the observed ammonium-mediated inhibition of RDX degradation. The results indicate that nitrogen availability is a
Michael J Quinn et al.
Ecotoxicology (London, England), 22(2), 231-239 (2012-11-20)
The purpose of this study was to assess the toxicological effects of two munition compounds, 4-amino-2,6-dinitrotoluene (4A-DNT) and 1,3,5-trinitro-1,3,5-triazine (RDX), on three different bird species: two common toxicological model species-the Northern Bobwhite (Colinus virginianus) and the Japanese Quail (Coturnix japonica)
Anat Bernstein et al.
Environmental science & technology, 47(1), 479-484 (2012-12-12)
The explosive Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) is known to be degraded aerobically by various isolates of the Rhodococcus species, with denitration being the key step, mediated by Cytochrome P450. Our study aimed at gaining insight into the RDX degradation mechanism by Rhodococcus
Karl K Irikura
The journal of physical chemistry. A, 117(10), 2233-2241 (2013-02-05)
The explosive nitramine RDX (1,3,5-trinitrohexahydro-s-triazine) is thought to decompose largely by homolytic N-N bond cleavage, among other possible initiation reactions. Density-functional theory (DFT) calculations indicate that the resulting secondary aminyl (R2N·) radical can abstract an oxygen atom from NO2 or
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