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Merck

45363

Supelco

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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About This Item

经验公式(希尔记法):
C11H23NOS
CAS号:
分子量:
217.37
Beilstein:
1770420
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

產品線

PESTANAL®

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

agriculture
environmental

格式

neat

SMILES 字串

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 密鑰

BMTAFVWTTFSTOG-UHFFFAOYSA-N

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相关类别

應用

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

推薦產品

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.

法律資訊

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

象形圖

Exclamation markEnvironment

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Inhalation - Aquatic Chronic 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

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


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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
M E Calderón-Segura et al.
Mutation research, 438(2), 81-88 (1999-02-26)
Molinate and butylate treatments for 4 h of Vicia faba root tip meristems, showed that both thiocarbamate herbicides increased significantly SCE frequency. Direct treatments of molinate and butylate on human lymphocytes applied 24 h after the beginning of culture did
Effects of carbofuran and the corn rhizosphere on growth of soil microorganisms.
M A Wootton et al.
Bulletin of environmental contamination and toxicology, 50(1), 49-56 (1993-01-01)

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