34333
氨氟灵
PESTANAL®, analytical standard
别名:
3-二乙基氨基-2,4-二硝基-6-三氟甲基苯胺
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关于此项目
经验公式（希尔记法）:
C11H13F3N4O4
化学文摘社编号:
分子量:
322.24
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
249-419-2
Beilstein/REAXYS Number:
2822138
MDL number:
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
SMILES string
CCN(CC)c1c(cc(c(N)c1[N+]([O-])=O)C(F)(F)F)[N+]([O-])=O
grade
analytical standard
product line
PESTANAL®
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
Quality Level
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Application
Dinitramine may be used as an analytical reference standard for the determination of the analyte in freshwater fish, soil and plant tissue, honey, fruit juice and wine, and food matrices 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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Aquatic Acute 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
农药列管产品
此项目有
Persistence of dinitramine and trifluralin in Nova Scotia, Canada.
K I Jensen et al.
Bulletin of environmental contamination and toxicology, 24(2), 238-243 (1980-02-01)
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)
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
Dinitramine. Residues in and toxicity to freshwater fish.
Olson LE, et al.
Journal of Agricultural and Food Chemistry, 23(3), 437-439 (1975)
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
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