Epoxy curing agent Knowledge Sodium thimerosal Ethylmercurithiosalicylic acid

Sodium thimerosal Ethylmercurithiosalicylic acid

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Sodium Thimerosal Structural Formula

Structural formula

Business number 016H
Molecular formula C9H9HgNaO2S
Molecular weight 404.81
label

thimerosal,

Thimerosal

Numbering system

CAS number:54-64-8

MDL number:MFCD00013062

EINECS number:200-210-4

RTECS number:OV8400000

BRN number:8169555

PubChem number:24900257

Physical property data

1. Character:Colorless crystal or milky white crystalline powder. Stable in air but not in sunlight


2. Density (g/mL,25/4): Undetermined


3. Relative vapor density (g /mL,AIR= 1): Undetermined


4. Melting point (ºC): Zhan232- 233


5. Boiling point (ºC,Normal pressure): Undetermined


6. Boiling point (ºC,5.2kPa): Undetermined


7. Refractive index: undetermined


8. Flashpoint (ºC):250


9. Specific optical rotation (º):Undetermined


10. Autoignition point or ignition temperature (ºC): Undetermined


11. Vapor pressure (kPa,25ºC): UndeterminedLog value of water) partition coefficient: Undetermined


17. Explosion limit (%,V/V): Undetermined


18. Lower explosion limit (%,V/V): Undetermined


19. Solubility:1gThe product is dissolved in About1mlWater, about8mlEthanol. Almost insoluble in ether and benzene. 1%Aqueous solutionpHAbout6.7. The solution can be addedETDAAs a stabilizer.

Toxicological data

None

Ecological data

None

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: 3

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 65.4

7. Number of heavy atoms: 14

8. Surface charge: 0

9. Complexity: 180

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: 2

Properties and stability

None

Storage method

None

Synthesis method

Prepared from the reaction of phosphorus thiol benzoic acid and ethylmercuric chloride

Purpose

is a disinfectant and antiseptic. It has bacteriostatic and mycobacterial effects and is more effective than mercurochrome. It is weaker than mercury chloride, less toxic and irritating. For external use as a skin and mucous membrane disinfectant. (Used for skin wound disinfection, eye and nose mucosal inflammation, urethral lavage, and skin fungal infections.)

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

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 65.4

7. Heavy Number of atoms: 14

8. Surface charge: 0

9. Complexity: 180

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: 2

Properties and stability

None

Storage method

None

Synthesis method

Prepared from the reaction of phosphorus thiol benzoic acid and ethylmercuric chloride

Purpose

is a disinfectant and antiseptic. It has bacteriostatic and mycobacterial effects and is more effective than mercurochrome. It is weaker than mercury chloride, less toxic and irritating. For external use as a skin and mucous membrane disinfectant. (Used for skin wound disinfection, eye and nose mucosal inflammation, urethral lavage, and skin fungal infections.)

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