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45469

Supelco

EPTC

PESTANAL®, analytical standard

Synonym(s):

S-Ethyl-N,N-dipropylthiocarbamate

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About This Item

Empirical Formula (Hill Notation):
C9H19NOS
CAS Number:
759-94-4
Molecular Weight:
189.32
Beilstein:
1762751
EC Number:
212-073-8
MDL number:
MFCD00053780
UNSPSC Code:
41116107
PubChem Substance ID:
329756762
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

CCCN(CCC)C(=O)SCC

InChI

1S/C9H19NOS/c1-4-7-10(8-5-2)9(11)12-6-3/h4-8H2,1-3H3

InChI key

GUVLYNGULCJVDO-UHFFFAOYSA-N

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Application

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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Legal Information

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK4026
BCBZ8663
SZBE118XV
SZB9126XV
SZE9126X

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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
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.
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
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)
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