45469
EPTC
PESTANAL®, analytical standard
别名:
S-乙基-N,N-二丙基硫代氨基甲酸酯
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关于此项目
经验公式（希尔记法）:
C9H19NOS
化学文摘社编号:
分子量:
189.32
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
212-073-8
Beilstein/REAXYS Number:
1762751
MDL number:
InChI key
GUVLYNGULCJVDO-UHFFFAOYSA-N
InChI
1S/C9H19NOS/c1-4-7-10(8-5-2)9(11)12-6-3/h4-8H2,1-3H3
SMILES string
CCCN(CCC)C(=O)SCC
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
相关类别
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin 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 1
flash_point_f
230.0 °F
flash_point_c
110 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
农药列管产品
此项目有
Dana M van Bemmel et al.
Environmental health perspectives, 116(11), 1541-1546 (2008-12-06)
The Agricultural Health Study (AHS) is a prospective cohort study of licensed pesticide applicators from Iowa and North Carolina enrolled between 1993 and 1997. EPTC (S-ethyl-N,N-dipropylthiocarbamate) is a thiocarbamate herbicide used in every region of the United States. The U.S.
A Vidal
Chemosphere, 36(12), 2593-2606 (1998-05-07)
Photocatalytic processes in the presence of titanium dioxide provide an interesting route to destroy hazardous organic contaminants, being operational in the UV-A domain with a potential use of solar radiation. In this paper, some specific contaminant classes of interest such
I Nagy et al.
Applied and environmental microbiology, 61(5), 2056-2060 (1995-05-01)
During atrazine degradation by Rhodococcus sp. strain N186/21, N-dealkylated metabolites and an hydroxyisopropyl derivative are produced. The cytochrome P-450 system that is involved in degradation of thiocarbamate herbicides by strain N186/21 (I. Nagy, G. Schoofs, F. Compernolle, P. Proost, J.
R E Staub et al.
Biochemical pharmacology, 58(9), 1467-1473 (1999-10-08)
Liver mitochondrial low-Km aldehyde dehydrogenase (ALDH2, EC 1.2.1.3), the isoform responsible for the conversion of acetaldehyde to acetate, is inhibited by the sulfoxide bioactivation products of Et2NC(O)SMe (from the alcohol aversion drug disulfiram), Pr2NC(O)SEt (the herbicide S-ethyl N,N-dipropylthiocarbamate), and BuNHC(O)SMe
Georgios Patakioutas et al.
Pest management science, 58(4), 352-362 (2002-04-27)
Five soils with different organic matter contents ranging from 0.48 to 10.4% were used to study the adsorption and desorption of alachlor, metolachor, EPTC, chlorothalonil and pirimiphos-methyl in batch experiments. The isotherm shapes according to Giles classification were S-type for
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