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Merck
CN

34333

Supelco

氨氟灵

PESTANAL®, analytical standard

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别名:
3-二乙基氨基-2,4-二硝基-6-三氟甲基苯胺
经验公式(希尔记法):
C11H13F3N4O4
CAS号:
分子量:
322.24
Beilstein:
2822138
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

格式

neat

SMILES字符串

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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应用

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.

法律信息

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

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Dermal - Aquatic Acute 1

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

农药列管产品

分析证书(COA)

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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)
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
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)
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

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