benzyltrimethylammonium chloride

admin news228Read

benzyltrimethylammonium chloride

structural formula

business number 00ju
molecular formula c10h16cln
molecular weight 185.70
label

n,n,n-trimethylphenylmethylammonium chloride,

trimethylbenzyl ammonium chloride,

emulsifier,

cellulose solvent,

polymerization inhibitor

numbering system

cas number:56-93-9

mdl number:mfcd00011782

einecs number:200-300-3

rtecs number:bo8400000

brn number:3917255

pubchem number:24848426

physical property data

1. properties: white or light yellow crystals, easy to absorb moisture.

2. density (g/ml, 20/4℃): 1.072

3. melting point (ºc): 239 (decomposition)

4. refraction rate (20ºc): 1.470

5. solubility: easily soluble in water, ethanol, hot benzene and butanol, slightly soluble in dibutyl phthalate and tributyl phosphate, insoluble in ether. irritating.

toxicological data

1. acute toxicity: rat oral ldlo: 250mg/kg; mouse oral ldlo: 1600mg/kg

2. irritating to eyes, respiratory system and skin.

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: 1

4. number of rotatable chemical bonds: 2

5. number of tautomers: none

6. topological molecule polar surface area 0

7. number of heavy atoms: 12

8. surface charge: 0

9. complexity: 107

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

hygroscopic. it is stable below 135℃ and decomposes into benzyl chloride and trimethylamine above 135℃. protective clothing should be worn when using.

storage method

this product should be sealed and stored in a cool, dry place.

synthesis method

the mixture of benzyl chloride, trimethylamine and methanol was refluxed for 4 hours, the methanol was evaporated to obtain a crude product, and the finished product benzyltrimethylammonium chloride was obtained through ethanol recrystallization with a yield of 88%.

purpose

reagents, emulsifiers, cellulose solvents, and polymerization inhibitors for the determination of platinum, palladium, mercury, and gold.

extended-reading:https://www.newtopchem.com/archives/category/products/page/122
extended-reading:https://www.morpholine.org/category/morpholine/page/5404/
extended-reading:https://www.newtopchem.com/archives/1002
extended-reading:https://www.bdmaee.net/wp-content/uploads/2020/06/67.jpg
extended-reading:https://www.newtopchem.com/archives/category/products/page/31
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/fascat2001-catalyst-cas301-10-0-stannous-octoate.pdf
extended-reading:https://www.bdmaee.net/wp-content/uploads/2022/08/38-2.jpg
extended-reading:https://www.newtopchem.com/archives/category/products/page/145
extended-reading:https://www.newtopchem.com/archives/748
extended-reading:https://www.newtopchem.com/archives/1853

admin
  • by Published on 2024-05-28 18:00:40
  • Reprinted with permission:https://www.morpholine.cc/15561.html
  • Benzyltrimethylammonium chloride
Comments  0  Guest  0