$l^{2}-stannane; phosphonato phosphate

Basic Information

$$l^{2}-stannane; phosphonato phosphate$

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CAS Number

15578-26-4

Molecular Formula

H4O14P4Sn2

Molecular Weight

589.34 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Agricultural Chemicals Pesticides Insecticides

Water Treatment Chemicals Coagulants and Flocculants Inorganic Coagulants

Basic Physical Properties

Melting Point

>400°C (dec.)

Boiling Point

°Cat760mmHg

Water Solubility

Insoluble in water.

SMILES

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[O-]P(=O)([O-])OP(=O)([O-])[O-].[O-]P(=O)([O-])OP(=O)([O-])[O-].[SnH2].[SnH2]

InChI

InChI=1S/2H4O7P2.2Sn.4H/c2*1-8(2,3)7-9(4,5)6;;;;;;/h2*(H2,1,2,3)(H2,4,5,6);;;;;;/p-8

InChIKey

RLPMUCMARRSJNH-UHFFFAOYSA-F

LogP

-8.5116

Topological Polar Surface Area

271.21999999999997 Å²

Hydrogen Bond Donor/Acceptor

0 / 14

Complexity

124

Safety Information

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Hazard Statement

H315 Causes skin irritation
Skin corrosion/irritation

H319 Causes serious eye irritation
Serious eye damage/eye irritation

H335 May cause respiratory irritation
Specific target organ toxicity, single exposure; Respiratory tract irritation

Synonyms & References

English

Tin (II) pyrophosphate
Stannous pyrophosphate
Tin(II) Pyrophosphat
TIN(II) PYROPHOSPHATE, hydrate
Tin II pyrophosphate, hydrate

MDL Number

MFCD00167376

Customs Code

2835399000

FAQ

What are the physical and chemical properties of $l^{2}-stannane; phosphonato phosphate (CAS: 15578-26-4)?

$l^{2}-Stannane; phosphonato phosphate is a solid compound with a crystalline form. Its molecular weight is approximately 325.46 g/mol. It is moderately soluble in water and has a low solubility in organic solvents. Chemically, it is highly reactive towards nucleophiles and can serve as a ligand in coordination compounds. It is stable under normal laboratory conditions but may react with reducing agents.

How is $l^{2}-stannane; phosphonato phosphate (CAS: 15578-26-4) typically synthesized?

$l^{2}-Stannane; phosphonato phosphate can be synthesized via a multistep process involving the reaction of stannylating agents with phosphonic acids. Commonly, triphenylphosphine and stannyl chloride are used as precursors. The synthesis typically requires the use of a Lewis acid catalyst to achieve high yield and selectivity. The process is usually carried out under anhydrous conditions to prevent hydrolysis.

What industries use $l^{2}-stannane; phosphonato phosphate (CAS: 15578-26-4)?

$l^{2}-Stannane; phosphonato phosphate finds applications in various industries, particularly in pharmaceuticals, where it acts as a ligand in metal complexes used for targeted drug delivery systems. It is also used in the development of sensors and semiconductors due to its unique chemical properties. Its use in polymer science is limited but explored for specific functionalities.

What precautions should be taken when handling $l^{2}-stannane; phosphonato phosphate (CAS: 15578-26-4)?

When handling $l^{2}-stannane; phosphonato phosphate (CAS: 15578-26-4), it is essential to wear appropriate personal protective equipment (PPE), including gloves, goggles, and a lab coat. Laboratory work should be conducted in a well-ventilated area or a fume hood to minimize inhalation risks. Spills should be cleaned up using appropriate absorbent materials and handled according to the Material Safety Data Sheet (MSDS) guidelines. Always refer to the current MSDS for the most up-to-date safety information.