Triphenyl antimony

Triphenyl antimony structural formula

Structural formula

Business number 067T
Molecular formula C18H15Sb
Molecular weight 353.07
label

triphenylantimony,

Antimony(III)triphenyl,

Triphenylstibine,

(C6H5)3Sb

Numbering system

CAS number:603-36-1

MDL number:MFCD00003000

EINECS number:24889648

RTECS number:WJ1400000

BRN number:3608108

PubChem number:210-037-6

Physical property data

Physical property data:
1. Character:White crystal

2. Relative density: 1.4343


3. Flashpoint ():>110


4. Melting point ():50


5. Boiling point (ºC):377 (decomposition)

Toxicological data

None

Ecological data

3. Ecological data:


1. Other harmful effects: This substance may be harmful to the environment and should be harmful to water bodies. Give special attention.

Molecular structure data

None

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 0

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 0

7. Number of heavy atoms: 19

8. Surface charge: 0

9. Complexity: 202

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Basic properties


White crystal. Stable in air. Soluble in most organic solvents, slightly soluble in ethanol, insoluble in water. Relative density1.4343 (1.4998). Melting point 50℃ (4663℃). Boiling point 377℃ (decomposition). Flash point>110℃. poisonous. Irritating.

Storage method

2. Storage


Keep sealed.

Synthesis method

None

Purpose

3. Purpose


Catalyst for the conversion of trienes into aromatics and hydrogenation of aromatics. Polymerization inhibitor. Lubricant additives. Dechlorination reaction.

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/29540

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