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Key Documents

Safety Information

45492

Supelco

Fentin chloride

PESTANAL®, analytical standard

Synonym(s):

Triphenyltin chloride, Chlorotriphenylstannane, Fentin chloride

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About This Item

Linear Formula:
(C6H5)3SnCl
CAS Number:
Molecular Weight:
385.47
Beilstein:
524762
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:

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

bp

240 °C/13.5 mmHg (lit.)

mp

108 °C (dec.) (lit.)

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

Cl[Sn](c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/3C6H5.ClH.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H;/q;;;;+1/p-1

InChI key

NJVOZLGKTAPUTQ-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

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Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - 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)

>302.0 °F

Flash Point(C)

> 150 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

农药列管产品

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G Janer et al.
The Journal of steroid biochemistry and molecular biology, 99(2-3), 147-156 (2006-04-20)
In a recent study, we demonstrated that androstenedione was mainly converted to testosterone (T) and 5alpha-dihydrotestosterone (DHT) by digestive gland/gonad complex microsomal fractions isolated from male Marisa cornuarietis, whereas it was primarily metabolized to 5alpha-dihydroandrostenedione (DHA) by females. In the
Toshihiro Horiguchi et al.
Analytical and bioanalytical chemistry, 396(2), 597-607 (2009-11-03)
To examine the role of the retinoid X receptor (RXR) in the development of imposex in gastropods, we investigated the time course of expression of the RXR gene in various tissues (ctenidium, ovary or testis, digestive gland, penis-forming area or
Yoshikazu Miura et al.
Toxicology, 299(2-3), 165-171 (2012-06-06)
Oral administration of triphenyltin chloride (TPT) (6 mg/100g body weight) inhibits insulin secretion by decreasing glucose-induced cytoplasmic Ca(2+) concentration ([Ca(2+)](i)) in pancreatic β-cells of the hamster. To test the possibility that the abnormal level of the [Ca(2+)](i) induced by TPT
Antonio Ortiz et al.
Biochimica et biophysica acta, 1720(1-2), 137-142 (2006-02-14)
Organotin compounds are widely distributed toxicants. They are membrane-active molecules with broad biological toxicity. In this contribution, we study the effect of triorganotin compounds on membrane permeability using phospholipid model membranes and human erythrocytes. Tribultyltin and triphenyltin are able to
Konstanze Grote et al.
Toxicology, 260(1-3), 53-59 (2009-05-26)
Consumers are exposed to organotin compounds (OTCs) via contaminated fish and seafood due to the accumulation of these compounds in marine organisms. Certain OTCs are immunotoxic and may also have endocrine disrupting properties resulting in adverse effects on the reproductive

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