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Merck
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Key Documents

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45469

Supelco

EPTC

PESTANAL®, analytical standard

Sinónimos:

S-Ethyl N,N-dipropylthiocarbamate

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About This Item

Fórmula empírica (notación de Hill):
C9H19NOS
Número de CAS:
759-94-4
Peso molecular:
189.32
Beilstein/REAXYS Number:
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.

Recommended products

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

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

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

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 1

flash_point_f

230.0 °F

flash_point_c

110 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (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
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
Z Q Shao et al.
Applied and environmental microbiology, 62(2), 403-407 (1996-02-01)
A cytochrome P-450 system in Rhodococcus strains, encoded by thcB, thcC, and thcD, participates in the degradation of thiocarbamates and several other pesticides. The regulation of the system was investigated by fusing a truncated lacZ in frame to thcB, the
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
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