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45704

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Vernolat

PESTANAL®, analytical standard

Synonym(e):

S-Propyl-dipropylthiocarbamat

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About This Item

Empirische Formel (Hill-System):
C10H21NOS
CAS-Nummer:
1929-77-7
Molekulargewicht:
203.34
Beilstein:
1767659
EG-Nummer:
217-681-7
MDL-Nummer:
MFCD00078733
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756913
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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

InChIKey

OKUGPJPKMAEJOE-UHFFFAOYSA-N

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Anwendung

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. Wirkung

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 .

Empfohlene Produkte

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.

Rechtliche Hinweise

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

Piktogramme

Exclamation markEnvironment
GHS07,GHS09

Signalwort

Warning

H-Sätze

H302,H410

Gefahreneinstufungen

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

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

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Analysenzertifikate (COA)

Lot/Batch Number
BCCG0824
BCBT4900
SZBC094XV
SZB7225XV
SZE7225X

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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
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
[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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