45363
Butylat
PESTANAL®, analytical standard
Synonym(s):
S-Ethyl N,N-diisobutylthiocarbamate
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All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C11H23NOS
CAS Number:
Molecular Weight:
217.37
Beilstein:
1770420
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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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
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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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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
Signal Word
Warning
Hazard Statements
Precautionary Statements
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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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.
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
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
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
R C Peffer et al.
Xenobiotica; the fate of foreign compounds in biological systems, 21(9), 1139-1152 (1991-09-01)
1. The metabolism of the thiocarbamate herbicide SUTAN (butylate) was studied after administration of single oral doses of [isobutyl-1-14C]SUTAN to male and female rats. 2. The radiolabelled dose was rapidly absorbed and excreted, with 79% of the dose excreted in
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