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Merck
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Documentos

45704

Supelco

Vernolat

PESTANAL®, analytical standard

Sinónimos:

S-Propyl dipropylthiocarbamate

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About This Item

Fórmula empírica (notación de Hill):
C10H21NOS
Número de CAS:
1929-77-7
Peso molecular:
203.34
Beilstein/REAXYS Number:
1767659
EC Number:
217-681-7
MDL number:
MFCD00078733
UNSPSC Code:
41116107
PubChem Substance ID:
329756913
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

CCCSC(=O)N(CCC)CCC

InChI

1S/C10H21NOS/c1-4-7-11(8-5-2)10(12)13-9-6-3/h4-9H2,1-3H3

InChI key

OKUGPJPKMAEJOE-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.
Vernolat is an herbicide, also known as S-Propyl dipropylthiocarbamate. It is a thiocarbamate compound that is also used as a general pesticide. It is commonly used to kill weeds in soybeans, peanuts and sweet potatoes .

Biochem/physiol Actions

Vernolat has been shown to inhibit aldehyde dehydrogenase (ALDH) in vivo . It is genotoxic by causing chromosomal changes such as chromatid exchanges and chromosomal aberrations in vitro .

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

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCG0824
BCBT4900
SZBC094XV
SZB7225XV
SZE7225X

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G B Quistad et al.
Life sciences, 55(20), 1537-1544 (1994-01-01)
The herbicide S-ethyl N,N-dipropylthiocarbamate (EPTC) and three of its candidate metabolites (the sulfoxide, N-depropyl and S-methyl derivatives) inhibit mitochondrial low-Km aldehyde dehydrogenase (ALDH) in liver by 56 to 82% 2 hr after these thiocarbamates are administered intraperitoneally (ip) to mice
A Pintér et al.
Annali dell'Istituto superiore di sanita, 25(4), 577-582 (1989-01-01)
Twenty-two herbicides were studied in 67 tests for induction of DNA damage, gene mutation and chromosomal changes in vitro and in vivo. Triazine and urea-type herbicides were found to be inactive in all but one test. Of 4 thiocarbamates, molinate
[Determination of maximum permissible exposure level for the herbicide vernam in the air of a working zone].
V N Karpenko et al.
Gigiena truda i professional'nye zabolevaniia, (9)(9), 49-50 (1983-09-01)
A Pintér et al.
Mutation research, 242(4), 279-283 (1990-12-01)
Three thiocarbamate herbicides, butylate (S-ethyl-diisobutylthiocarbamate), vernolate (S-propyl dipropylthiocarbamate) and molinate (S-ethyl-N,N-hexamethylenethiocarbamate) were assayed for cytogenetic effect in the mouse bone marrow micronucleus test. Butylate was inactive in bone marrow, vernolate caused a marginal increase in the incidence of micronucleated polychromatic

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