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ERR-001S

Supelco

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:
Molecular Weight:
222.12
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24

grade

certified reference material

Quality Level

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

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

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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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
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
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)
Hao-Ping Chen et al.
Applied and environmental microbiology, 78(21), 7798-7800 (2012-08-28)
Whole-genome sequencing, transcriptomic analyses, and metabolic reconstruction were used to investigate Gordonia sp. strain KTR9's ability to catabolize a range of compounds, including explosives and steroids. Aspects of this mycolic acid-containing actinobacterium's catabolic potential were experimentally verified and compared with
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

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