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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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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)
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
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 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
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.
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