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45491

Supelco

Fentin acetate

PESTANAL®, analytical standard

Synonym(s):

Triphenyltin acetate, Acetoxytriphenylstannane

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About This Item

Linear Formula:
(C6H5)3SnOCOCH3
CAS Number:
900-95-8
Molecular Weight:
409.07
Beilstein/REAXYS Number:
4146107
EC Number:
212-984-0
MDL number:
MFCD00014977
UNSPSC Code:
41116107
PubChem Substance ID:
329756783

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
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

storage temp.

2-8°C

SMILES string

CC(=O)O[Sn](c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/3C6H5.C2H4O2.Sn/c3*1-2-4-6-5-3-1;1-2(3)4;/h3*1-5H;1H3,(H,3,4);/q;;;;+1/p-1

InChI key

WDQNIWFZKXZFAY-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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Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
SZBA266XV
SZE7050X
7050X
0286X
4055X

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J H Yen et al.
Ecotoxicology and environmental safety, 49(2), 164-170 (2001-06-02)
The effects of various factors on fungicide triphenyltin acetate dissipation in selected soil types were studied; temperature is clearly the most important factor of these. Residues of this fungicide in Fangtzupo clay loam and Lanyang loam incubated at 30 degrees
M Dacasto et al.
Pharmacological research, 29(2), 179-186 (1994-02-01)
To perform a better investigation of the toxic activity of triphenyltin acetate (TPTA) already described in vivo, primary cultures of murine thymocytes were incubated for 2 to 32 h with graded amounts (0.5-8 microM) of the triorganotin compound. The cytotoxic
M Dacasto et al.
Toxicology, 169(3), 227-238 (2001-11-24)
Organotin compounds (OTs) find application worldwide as catalysts, stabilizers and biocides. Triphenyltin derivatives (TPs), including the fungicide triphenyltin acetate (TPTA), are OTs mostly used in our country. Some OTs were proved to be immunotoxic and in this paper the cytotoxicity
C Nebbia et al.
Journal of toxicology and environmental health. Part A, 56(6), 433-447 (1999-03-30)
The in vitro effects of the organotin (OT) compound triphenyltin acetate (TPTA) on cytochrome P-450 content and functions were investigated in liver microsomes from untreated, phenobarbital (PB)- or beta-naphthoflavone- (betaNAF) pretreated rats. At a concentration of 0.5 mM, TPTA caused
J L Lin et al.
American journal of nephrology, 13(2), 124-128 (1993-01-01)
Three patients who developed acute nephropathy following ingestion of triphenyltin acetate (TPTA) are described. All of them had significant proteinuria, azotemia, and polyuria. Mild neurological manifestations in all patients were also noted. Hematuria and pyuria were noted in 1 severely
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