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Merck
CN

45492

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:
639-58-7
Molecular Weight:
385.47
EC Number:
211-358-4
UNSPSC Code:
41116107
PubChem Substance ID:
329756784
Beilstein/REAXYS Number:
524762
MDL number:
MFCD00000519

Key Documents

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InChI key

NJVOZLGKTAPUTQ-UHFFFAOYSA-M

InChI

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

SMILES string

Cl[Sn](c1ccccc1)(c2ccccc2)c3ccccc3

grade

analytical standard

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

Quality Level

100

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

signalword

Danger

Hazard Classifications

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

Storage Class

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

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCG5124
BCBW6509
BCBS3732V

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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
Angeliki Lyssimachou et al.
Aquatic toxicology (Amsterdam, Netherlands), 89(2), 129-135 (2008-07-25)
Long-term exposures to organotin compounds have shown alterations on endogenous steroid levels in gastropods together with the development of imposex. However, information regarding short-term effects of these compounds on the endocrine system of gastropods is lacking. This work aimed at
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