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Merck
CN

45633

Supelco

环丙氟

PESTANAL®, analytical standard

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About This Item

经验公式(希尔记法):
C14H16F3N3O4
CAS号:
分子量:
347.29
Beilstein:
2179006
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®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

包装形式

neat

SMILES字符串

CCCN(CC1CC1)c2c(cc(cc2[N+]([O-])=O)C(F)(F)F)[N+]([O-])=O

InChI

1S/C14H16F3N3O4/c1-2-5-18(8-9-3-4-9)13-11(19(21)22)6-10(14(15,16)17)7-12(13)20(23)24/h6-7,9H,2-5,8H2,1H3

InChI key

ITVQAKZNYJEWKS-UHFFFAOYSA-N

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相关类别

应用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

法律信息

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

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象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 2

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

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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访问文档库

A R Jacobson et al.
Chemical research in toxicology, 1(5), 304-311 (1988-09-01)
Fluorine NMR spectroscopy has been used to identify and quantitate metabolites of profluralin appearing in the urine of rats postingestion of the herbicide. The chemical shift of the trifluoromethyl group was shown to be a useful indicator of the chemical
N D Camper et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 15(5), 457-473 (1980-01-01)
The degradation of profluralin [N-(cyclopropylmethyl)-alpha,alpha,alpha-trifluoro-2,6-dinitro-N-propyl-p-toluidine] and trifluralin (alpha,alpha,alpha-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine) was studied under aerobic and anaerobic soil conditions. Three soils (Goldsboro loamy sand, Cecil loamy sand, Drummer clay loam) were each treated with 1 ppmw herbicide; anaerobic conditions were maintained by flooding.
R C Honeycutt et al.
Journal of environmental pathology and toxicology, 3(5-6), 21-33 (1980-06-01)
Recent developments in the technology of removal and characterization of bound residues of two herbicides, nitrofen and profluralin, from plants and soil will be reviewed. 14C-Nitrofen was found to be metabolized into starch in wheat grain as well as bound
M J Arrowood et al.
FEMS microbiology letters, 136(3), 245-249 (1996-03-01)
Despite the evaluation of over 100 antimicrobial drugs, the diarrheal disease cryptosporidiosis has remained refractory to treatment. We report the evaluation of five dinitroaniline herbicides including trifluralin, profluralin, nitralin, pendimethalin, and fluchloralin for anticryptosporidial activity in an in vitro cultivation
T R Edgerton et al.
Journal of analytical toxicology, 9(1), 15-19 (1985-01-01)
A method is presented for the analysis of trace amounts of dinitroaniline herbicides in tissue and excreta. The method employs extraction of the tissue or excreta with organic solvent, clean up by liquid/liquid partitioning or silica gel chromatography, and ultimate

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