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45411

Supelco

Cyhexatin

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C18H34OSn
CAS Number:
13121-70-5
Molecular Weight:
385.17
Beilstein:
6099492
EC Number:
236-049-1
MDL number:
MFCD00078642
UNSPSC Code:
41116107
PubChem Substance ID:
329756710
Pricing and availability is not currently available.

grade

analytical standard

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

storage temp.

2-8°C

SMILES string

O[Sn](C1CCCCC1)(C2CCCCC2)C3CCCCC3

InChI

1S/3C6H11.H2O.Sn/c3*1-2-4-6-5-3-1;;/h3*1H,2-6H2;1H2;/q;;;;+1/p-1

InChI key

WCMMILVIRZAPLE-UHFFFAOYSA-M

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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.

Legal Information

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

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H301,H312 + H332,H410

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

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

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P Hrelia et al.
Mutation research, 321(4), 219-228 (1994-06-01)
Cyanazine, cyhexatin, dicamba and DNOC are pesticides commonly and broadly used in agriculture pest control. However, there is little information on their toxicity and mutagenicity in human cells and in whole animals. Therefore, UDS assay and SCE assay in human
K I Sahib et al.
Journal of biochemical toxicology, 1(4), 55-66 (1986-12-01)
Previous studies from this laboratory have indicated that tricyclohexyltin hydroxide (Plictran) is a potent inhibitor of both basal- and isoproterenol-stimulated cardiac sarcoplasmic reticulum (SR) Ca2+-ATPase, with an estimated IC-50 of 2.5 X 10(-8) M. The present studies were initiated to
[Determination of the active principle of a plictran preparation and its metabolites in environmental objects].
Iu A Buniatian et al.
Gigiena i sanitariia, (3)(3), 55-57 (1983-03-01)
K S Rao et al.
Journal of biochemical toxicology, 2, 125-140 (1987-01-01)
Tricyclohexylhydroxytin, commonly known as Plictran, inhibited Na+, K+-ATPase activity of rat brain synaptosomes in a concentration-dependent manner with median inhibitory concentration (IC-50) of 2 microM. Both K+-stimulated para-nitrophenylphosphatase and [3-H]-ouabain binding to synaptosomes were also inhibited by Plictran with IC-50
[Experimental determination of the maximum allowable concentration of the acaricide plictran in the air of the work zone].
A E Tatevosian et al.
Gigiena truda i professional'nye zabolevaniia, (5)(5), 52-53 (1984-05-01)
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