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Merck
CN

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

Key Documents

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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.

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
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

Regulatory Information

农药列管产品

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG0631
BCBT4910

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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 2,4-D butylate herbicides on thyroid gland and testis of mice].
Huai-fu Wang et al.
Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases, 24(6), 375-376 (2006-07-11)
Shannon M Lynch et al.
Environmental research, 109(7), 860-868 (2009-07-21)
Although limited, epidemiologic studies suggest possible associations between butylate use and cancer risk, specifically prostate cancer and non-Hodgkin lymphoma (NHL). We examined butylate use and cancer risk more broadly in the AHS, a cohort of licensed pesticide applicators in Iowa
Hongyun Huang et al.
Cell transplantation, 15(8-9), 799-809 (2007-02-03)
To engineer liver tissues with a clinically significant size, in vivo evaluation of performance using large-scale animal studies are necessary before proceeding to human clinical trials. As pigs are the most suitable candidates, the development of culture conditions suitable for
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