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Merck
CN

45704

Supelco

灭草猛

PESTANAL®, analytical standard

别名:

S-丙基二丙基硫代氨基甲酸酯

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About This Item

经验公式(希尔记法):
C10H21NOS
CAS号:
分子量:
203.34
Beilstein:
1767659
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

包装形式

neat

SMILES字符串

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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应用

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 .

生化/生理作用

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 .

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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.

法律信息

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

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象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

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

储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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

法规信息

农药列管产品

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分析证书(COA)

Lot/Batch Number

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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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