Gallamine Triethiodide Gallamine Triethiodide
Structural formula
| Business number | 01DP |
|---|---|
| Molecular formula | C30H60I3N3O3 |
| Molecular weight | 891.54 |
| label |
triiodoquaternary ammonium phenol |
Numbering system
CAS number:65-29-2
MDL number:MFCD00011832
EINECS number:200-605-1
RTECS number:BS1100000
BRN number:None
PubChem number:24277837
Physical property data
1. Character:White or milky white crystalline powder, odorless, slightly bitter, hygroscopic
2. Density (g/mL,25/4℃): Unsure
3. Relative vapor density (g/mL,AIR=1): Unsure
4. Melting point (ºC):235 (dec.)(lit.)
5. Boiling point (ºC,Normal pressure): Uncertain
6. Boiling point (ºC, 5.2kPa): Unsure
7. Refractive index:Not sure
8. Flash point (ºC): Unsure
9. Specific optical rotation (º): Unsure
10. Autoignition point or ignition temperature (ºC): Unsure
11. Vapor pressure (kPa,25ºC): Unsure
12. 17. Explosion limit (%, V/V): Unsure
18. Lower explosion limit (%,V/V): Unsure
19. Solubility:Easily soluble in water(1：6), slightly soluble in Ethanol(1：500), acetone, benzene and chloroform, insoluble in ether
Toxicological data
None yet
Ecological data
None yet
Molecular structure data
None yet
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: 6
4. Number of rotatable chemical bonds: 21
5. Number of tautomers: none
6. Topological molecule polar surface area 27.7
7. Number of heavy atoms: 39
8. Surface charge: 0
9. Complexity: 489
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: 4
Properties and stability
None yet
Storage method
This product should be sealed in4℃Save in a dry place and away from light.
Synthesis method
Pyrogallic acid forms a sodium salt under the action of sodium acetate , and then reacted with diethylaminoethyl chloride and ethyl iodide in sequence.
Purpose
For biochemical research. medicine.
eft> This product should be sealed in 4℃Keep dry and away from light.
Synthesis method
Pyrogallic acid forms a sodium salt under the action of sodium acetate , and then reacted with diethylaminoethyl chloride and ethyl iodide in sequence.
Purpose
For biochemical research. medicine.
