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45363

Supelco

Butylat

PESTANAL®, analytical standard

Synonym(s):

S-Ethyl N,N-diisobutylthiocarbamate

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About This Item

Empirical Formula (Hill Notation):
C11H23NOS
CAS Number:
2008-41-5
Molecular Weight:
217.37
Beilstein:
1770420
EC Number:
217-916-3
MDL number:
MFCD00055338
UNSPSC Code:
41116107
PubChem Substance ID:
329756673
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

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

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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.

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Legal Information

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

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H332,H411

Precautionary Statements

P273 - P304 + P340 + P312

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG0631
BCBT4910
SZBC095XV
SZB7225XV
SZE7225X

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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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