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34333

Supelco

Dinitramine

PESTANAL®, analytical standard

Synonym(s):

3-Diethylamino-2,4-dinitro-6-trifluoromethylaniline

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About This Item

Empirical Formula (Hill Notation):
C11H13F3N4O4
CAS Number:
Molecular Weight:
322.24
Beilstein/REAXYS Number:
2822138
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CCN(CC)c1c(cc(c(N)c1[N+]([O-])=O)C(F)(F)F)[N+]([O-])=O

InChI

1S/C11H13F3N4O4/c1-3-16(4-2)9-7(17(19)20)5-6(11(12,13)14)8(15)10(9)18(21)22/h5H,3-4,15H2,1-2H3

InChI key

OFDYMSKSGFSLLM-UHFFFAOYSA-N

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Application

Dinitramine may be used as an analytical reference standard for the determination of the analyte in freshwater fish,[1] soil and plant tissue,[2] honey, fruit juice and wine,[3] and food matrices[4] by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation markEnvironment

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Warning

hcodes

Hazard Classifications

Acute Tox. 4 Dermal - Aquatic Acute 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Bharat Bhushan et al.
Biochemical and biophysical research communications, 306(2), 509-515 (2003-06-14)
Enzyme catalyzed biotransformation of the energetic chemical octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) is not known. The present study describes a xanthine oxidase (XO) catalyzed biotransformation of HMX to provide insight into the biodegradation pathway of this energetic chemical. The rates of biotransformation under
Multi-residue method for the determination of 450 pesticide residues in honey, fruit juice and wine by double-cartridge solid-phase extraction/gas chromatography-mass spectrometry and liquid chromatography-tandem mass spectrometry.
Pang GF, et al.
Food Additives and Contaminants, 23(8), 777-810 (2006)
Determination of dinitramine residues in soil and plant tissue.
Newsom HC and Mitchell EM
Journal of Agricultural and Food Chemistry, 20(6), 1222-1224 (1972)
Annamaria Halasz et al.
Environmental science & technology, 36(4), 633-638 (2002-03-07)
In an earlier study, we reported that hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) biodegraded with domestic anaerobic sludge to produce a key RDX ring cleavage intermediate that was tentatively identified as methylenedinitramine (O2NNHCH2NHNO2) using LC/MS with negative electrospray ionization (ES-). Recently, we obtained a
Dinitramine. Residues in and toxicity to freshwater fish.
Olson LE, et al.
Journal of Agricultural and Food Chemistry, 23(3), 437-439 (1975)

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