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经验公式(希尔记法):
C11H14ClNO
化学文摘社编号:
分子量:
211.69
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
217-638-2
Beilstein/REAXYS Number:
2103903
MDL number:
产品名称
毒草胺, PESTANAL®, analytical standard
InChI key
MFOUDYKPLGXPGO-UHFFFAOYSA-N
InChI
1S/C11H14ClNO/c1-9(2)13(11(14)8-12)10-6-4-3-5-7-10/h3-7,9H,8H2,1-2H3
SMILES string
CC(C)N(C(=O)CCl)c1ccccc1
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
Quality Level
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Application
Propachlor may be used as an analytical reference standard for the quantification of the analyte in industrial wastewater samples and complex matrices using chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
General description
Propachlor is a herbicide, widely used in oil seeds and crop planting.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Sens. 1
存储类别
6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
危险化学品
农药列管产品
此项目有
Liquid-liquid extraction for sample preparation prior to gas chromatography and gas chromatography-mass spectrometry determination of herbicide and pesticide compounds
Mahara.MB, et al.
Microchemical Journal, Devoted to the Application of Microtechniques in All Branches of Science, 58(1), 31-38 (1998)
Multiresidue analysis of 240 pesticides in apple and lettuce by QuEChERS sample preparation and HPLC-MS/MS analysis
Wang.L, et al.
The Korean Journal of Pesticide Science, 46(5), 424-429 (2008)
C S Liu et al.
Chemosphere, 85(9), 1438-1443 (2011-09-07)
Chloroacetanilide herbicides are extensively used in the control of weeds and have widely resulted in nonpoint contamination of groundwater and soil resources. In the attempt to achieve better remediation for herbicide-contaminated resources, we investigated the reductive transformation of propachlor through
Katrice A Lippa et al.
Environmental toxicology and chemistry, 24(10), 2401-2409 (2005-11-05)
Second-order rate constants (kNuc) for aqueous-phase bimolecular nucleophilic substitution (SN2) reactions of a range of anionic nucleophiles with alachlor, propachlor, and two analogs of propachlor (a thioacetanilide and a beta-anilide) were fit to the Swain-Scott and Edwards models. Correlations of
P J Dierickx
Cell biology and toxicology, 15(5), 325-332 (2000-05-17)
Alachlor, metolachlor, and propachlor are widely used chloroacetanilide herbicides. Their cytotoxicity in rat (Fa32) and human (Hep G2) hepatoma-derived cells was investigated, in connection with their influence on the endogenous glutathione (GSH) content, on the xenobiotic-metabolizing phase I enzymes 7-ethoxyresorufin
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