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Merck
CN

45363

丁草特

PESTANAL®, analytical standard

别名:

S-乙基-N,N-二异丁基硫代氨基甲酸酯

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关于此项目

经验公式(希尔记法):
C11H23NOS
化学文摘社编号:
分子量:
217.37
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
217-916-3
Beilstein/REAXYS Number:
1770420
MDL number:
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grade

analytical standard

Quality Level

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

CCSC(=O)N(CC(C)C)CC(C)C

InChI

1S/C11H23NOS/c1-6-14-11(13)12(7-9(2)3)8-10(4)5/h9-10H,6-8H2,1-5H3

InChI key

BMTAFVWTTFSTOG-UHFFFAOYSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

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

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 2

存储类别

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

法规信息

农药列管产品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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T Umemura et al.
Journal of cancer research and clinical oncology, 127(10), 583-590 (2001-10-16)
Transgenic mice carrying the human prototype c-Ha-ras gene (rasH2 mice) are highly susceptible to lung carcinogens. In order to investigate the possibility of developing a rapid in vivo assay for lung carcinogens, we examined whether the tumor-promoting activity of butylhydroxytoluene
Jonathan Clayden et al.
Chemical communications (Cambridge, England), (13)(13), 1393-1394 (2006-03-22)
Directed metallation and sulfinylation yields sulfoxides which undergo ipso nucleophilic aromatic substitution with tertiary and secondary alkyllithiums, giving aromatic rings bearing alkyl groups generally incompatible with directed metallation methods and with regioselectivity complementary with classical Friedel-Crafts substitution.
V T Kasumov et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(13), 3037-3047 (2004-10-13)
A series of sterically hindered N-arylsalicylaldimines (SAs) previously prepared from substituted salicylaldehydes (X-Sal, where X = H, Cl, Br, NO2, OH, OCH3) and 2,6-di-t-butyl-1-hydroxyaniline (LxH) and 2,5-di-t-butylaniline (Lx'H) were characterized by 1H and 13C NMR, UV-Vis and electrochemical methods. The



全球贸易项目编号

货号GTIN
45363-250MG04061837625213