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Merck

PS1031

Fentin hydroxide

analytical standard

Synonym(s):

Triphenyltin hydroxide

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About This Item

Empirical Formula (Hill Notation):
C18H16OSn
CAS Number:
Molecular Weight:
367.03
EC Number:
200-990-6
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
4139186
MDL number:
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grade

analytical standard

packaging

ampule of 500 mg

manufacturer/tradename

Chem Service, Inc. PS-1031

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

SMILES string

O[Sn](c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/3C6H5.H2O.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H2;/q;;;;+1/p-1

InChI key

BFWMWWXRWVJXSE-UHFFFAOYSA-M

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

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

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Marcia Sarpa et al.
Journal of toxicology and environmental health. Part A, 73(13-14), 965-971 (2010-06-22)
Fentin or triphenylthin (TPT) is an organotin compound (OTC) widely used as an agricultural fungicide and miticide. It is well known that TPT exerts adverse effects on the reproductive and immune systems and may disrupt the endocrine system, raising concerns
Immunotoxicity of pesticides.
J G Vos et al.
Developments in toxicology and environmental science, 11, 229-240 (1983-01-01)
Fungicide residues. Part VII. Determination of residues of fentin in vegetables and cocoa products by spectrofluorimetry.
P G Baker et al.
The Analyst, 105(1248), 282-285 (1980-03-01)
David I Shapiro-Ilan et al.
Environmental entomology, 40(1), 59-65 (2011-12-21)
Hypocreales fungi such as Beauveria bassiana (Balsamo) Vuillemin and Metarhizium brunneum Petch can be negatively affected by fungicides thereby reducing their biocontrol potential. In a previous study, we demonstrated enhanced fungicide resistance in B. bassiana through artificial selection. However, it
S Tanimoto et al.
Molecular reproduction and development, 39(4), 409-414 (1994-12-01)
Flux of K+ and changes in intracellular Ca2+ in the sperm of salmonid fishes were measured with spectrophotometry, ion electrode, microscopic fluorometry, and radioisotope accumulation. Release of K+ occurred at the initiation of sperm motility which is induced by decrease

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