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45493

Supelco

Fentin hydroxide

PESTANAL®, analytical standard

Sinónimos:

Triphenyltin hydroxide

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About This Item

Fórmula empírica (notación de Hill):
C18H16OSn
Número de CAS:
76-87-9
Peso molecular:
367.03
Beilstein/REAXYS Number:
4139186
EC Number:
200-990-6
MDL number:
MFCD00013928
UNSPSC Code:
41116107
PubChem Substance ID:
329756785
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

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

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Categorías relacionadas

General description

Fentin hydroxide is a non-systemic fungicide that helps in controlling fungal disease in potatoes, sugar beet, and hops.

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

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCJ8550
BCBX5218
SZBD281XV
SZBA266XV
SZE7050X

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[Species differences in the sensitivity to the diabetogenic action of triphenyltin hydroxide].
H Matsui et al.
Sangyo igaku. Japanese journal of industrial health, 25(3), 190-191 (1983-05-01)
Eduardo C Oliveira-Filho et al.
Chemosphere, 81(2), 218-227 (2010-07-03)
Plant molluscicides have been regarded as possible alternatives to the costly and environmentally hazardous molluscicides currently available. This study was undertaken to compare the developmental toxicity of a plant molluscicide (Euphorbia milii latex, LAT) with that of three synthetic molluscicidal
Marcia Sarpa et al.
Regulatory toxicology and pharmacology : RTP, 49(1), 43-52 (2007-07-10)
Triphenyltin-hydroxide (TPTH) is used as agricultural fungicide in Brazil and elsewhere. This study was undertaken to evaluate the developmental toxicity of TPTH in mice. Swiss Webster mice were treated by gavage with TPTH (0, 3.75, 7.5, 15 and 30 mg/kg
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
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
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