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
I Nagy et al.
Journal of bacteriology, 177(3), 676-687 (1995-02-01)
Determination of the N-terminal sequences of two EPTC (S-ethyl dipropylcarbamothioate)-induced proteins from thiocarbamate-degrading Rhodococcus sp. strain NI86/21 resolved by two-dimensional electrophoresis enabled the localization of the respective structural genes on two distinct DNA fragments. One of these strongly induced proteins
A C Tam et al.
Applied and environmental microbiology, 53(5), 1088-1093 (1987-05-01)
Arthrobacter sp. strain TE1 isolated from s-ethyl-N,N-dipropylthiocarbamate (EPTC)-exposed soil degraded this herbicide effectively and could grow on EPTC as the sole carbon source. TE1 harboured four plasmids of 65.5, 60, 50.5, and 2.5 megadaltons. Spontaneous mutants unable to degrade EPTC
Comparison of the persistence of EPTC, metribuzin, and propanil in Saskatchewan field soils.
A E Smith et al.
Bulletin of environmental contamination and toxicology, 29(2), 243-247 (1982-08-01)
J R Cashman et al.
Chemical research in toxicology, 2(6), 392-399 (1989-11-01)
The in vitro liver microsomal oxidation of eptam (ethyl N,N-dipropylthiocarbamate) in the presence of freshwater and salt water adapted striped bass liver microsomes was investigated. In freshwater hepatic microsomes from striped bass, eptam is S-oxygenated in a process consistent with
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
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