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Tetraphenyltin

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Tetraphenyltin Basic information

Product Name:
Tetraphenyltin
Synonyms:
  • Tetraphenyltin, min. 95%
  • Tetraphenyltin,95%
  • Tetraphenyltin,97%
  • Tetraphenyltin,min.95%
  • Ph4Sn
  • SnPh4
  • TIN TETRAPHENYL
  • TETRAPHENYLTIN
CAS:
595-90-4
MF:
C24H20Sn
MW:
427.13
EINECS:
209-872-9
Product Categories:
  • Classes of Metal Compounds
  • Sn (Tin) Compounds
  • Typical Metal Compounds
  • organotin compound
  • Chemical Synthesis
  • Organometallic Reagents
  • Organotin
  • Organotins
Mol File:
595-90-4.mol
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Tetraphenyltin Chemical Properties

Melting point:
224-227 °C(lit.)
Boiling point:
420 °C
Density 
1,49 g/cm3
vapor density 
14.7 (vs air)
Flash point:
231 °F
solubility 
insoluble in Ether
form 
Powder
color 
white
Specific Gravity
1.49
Water Solubility 
INSOLUBLE
Hydrolytic Sensitivity
1: no significant reaction with aqueous systems
BRN 
3145842
Exposure limits
ACGIH: TWA 0.1 mg/m3; STEL 0.2 mg/m3 (Skin)
NIOSH: IDLH 25 mg/m3; TWA 0.1 mg/m3
Stability:
Stable. Incompatible with strong acids, strong oxidizing agents.
InChIKey
CRHIAMBJMSSNNM-UHFFFAOYSA-N
CAS DataBase Reference
595-90-4(CAS DataBase Reference)
NIST Chemistry Reference
Stannane, tetraphenyl-(595-90-4)
EPA Substance Registry System
Stannane, tetraphenyl- (595-90-4)
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Safety Information

Hazard Codes 
T,N
Risk Statements 
23/24/25-50/53
Safety Statements 
26-27-28-45-60-61-36/37/39-28A
RIDADR 
UN 3146 6.1/PG 3
WGK Germany 
3
TSCA 
Yes
HS Code 
2931.90.6000
HazardClass 
6.1
PackingGroup 
III

MSDS

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Tetraphenyltin Usage And Synthesis

Chemical Properties

White powder. Insoluble in water; soluble in hot benzene, toluene, xylene.

Uses

Stabilizer in chlorinated transformer oils, mothproofing agent, scavenger in dielectric fluids, intermediate.

Uses

Tetraphenyltin is used as stabilizer, catalyze, adhesion agent, it is used to produce other chemicals like, it can react with 3-chloro-2,5-diisobutyl-pyrazine to get 3,6-diisobutyl-2-phenylpyrazine. It is used as starting materials or catalysts.

Hazard

Skin irritant.

Purification Methods

It forms yellow crystals from CHCl3, pet ether (b 77-120o), xylene or *benzene/cyclohexane, and is dried at 75o/20mm. [Gilman & Rosenberg J Am Chem Soc 74 531 1952, Beilstein 16 IV 1592.]

TetraphenyltinSupplier

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