Conditions | Yield |
---|---|
With ethanol at 100℃; | |
at 120℃; | |
In water at 20℃; | |
In chloroform; toluene at 20℃; Solvent; Temperature; Autoclave; | 405.5 g |
glycidyltrimethylammonium chloride
Conditions | Yield |
---|---|
With sodium hydroxide In water at 20℃; for 0.5h; | |
With sodium hydroxide In water | |
With sodium hydroxide at 13 - 15℃; for 1.16667h; | |
With sodium hydroxide |
Conditions | Yield |
---|---|
With sodium chloride; sodium hydroxide In isopropyl alcohol at 20 - 40℃; for 7h; pH=11; | 96% |
glycidyltrimethylammonium chloride
Conditions | Yield |
---|---|
In water for 0.166667h; | 90% |
Conditions | Yield |
---|---|
for 0.166667h; | 90% |
glycidyltrimethylammonium chloride
Conditions | Yield |
---|---|
In water for 0.166667h; | 90% |
glycidyltrimethylammonium chloride
Conditions | Yield |
---|---|
In water for 0.166667h; | 90% |
glycidyltrimethylammonium chloride
Conditions | Yield |
---|---|
In water for 10h; | 87.8% |
Conditions | Yield |
---|---|
In water at 60℃; | 87% |
glycidyltrimethylammonium chloride
1,14-diamino-3,6,9,12-tetraoxatetradecane
Conditions | Yield |
---|---|
Stage #1: C17H6Br2Cl2N4O2; 1,14-diamino-3,6,9,12-tetraoxatetradecane With sodium carbonate at 35 - 40℃; for 2h; pH=5-6; Stage #2: glycidyltrimethylammonium chloride With hydrogenchloride at 85℃; pH=4; | 82.46% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In isopropyl alcohol; acetone at 80℃; for 16h; | 79% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In isopropyl alcohol; acetone at 80℃; for 16h; | 79% |
1-(4,6-dichloro-[1,3,5]triazin-2-ylamino)-anthraquinone
glycidyltrimethylammonium chloride
1,14-diamino-3,6,9,12-tetraoxatetradecane
Conditions | Yield |
---|---|
Stage #1: 1-(4,6-dichloro-[1,3,5]triazin-2-ylamino)-anthraquinone; 1,14-diamino-3,6,9,12-tetraoxatetradecane With sodium carbonate at 35 - 40℃; for 2h; pH=5-6; Stage #2: glycidyltrimethylammonium chloride With hydrogenchloride at 85℃; pH=4; | 79% |
3-hydroxyethylammonium-n-propanesulfonate
glycidyltrimethylammonium chloride
N-(2-hydroxy-3-trimethylammoniumpropyl)-N-(2-hydroxyethyl)homotaurine inner salt
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In ethanol; water at 5 - 20℃; for 21h; | 76% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In isopropyl alcohol; acetone at 80℃; for 16h; | 76% |
2-benzyloxybenzoic acid
glycidyltrimethylammonium chloride
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In isopropyl alcohol; acetone at 80℃; for 16h; | 73% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In isopropyl alcohol; acetone at 80℃; for 16h; | 70% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 60℃; for 2h; | 60% |
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 120℃; for 16h; | 57% |
glycidyltrimethylammonium chloride
heptakis(6-amino-6-deoxy)-β-cyclodextrin
Conditions | Yield |
---|---|
In aq. buffer at 50℃; for 24h; pH=10; | 51% |
guanidine sulfamate
glycidyltrimethylammonium chloride
Conditions | Yield |
---|---|
With water; 4-pyrrolidin-1-ylpyridine at 45℃; for 2h; Temperature; | 50.5% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In isopropyl alcohol; acetone at 60℃; for 16h; | 26% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In isopropyl alcohol; acetone at 60℃; for 16h; | 25% |
Conditions | Yield |
---|---|
With sodium hydroxide at 50℃; | 23% |
bis(2-propyl)-p-toluenesulfonyloxymethylphosphonate
glycidyltrimethylammonium chloride
Conditions | Yield |
---|---|
Multistep reaction; |
bis(2-propyl)-p-toluenesulfonyloxymethylphosphonate
glycidyltrimethylammonium chloride
2,6-diaminopurine
Conditions | Yield |
---|---|
Multistep reaction; |
Conditions | Yield |
---|---|
With sodium hydroxide Product distribution; var. conditions; also degradation of γ-cyclodextrin; |
bis(2-propyl)-p-toluenesulfonyloxymethylphosphonate
glycidyltrimethylammonium chloride
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
With ammonium hydroxide; trimethylsilyl bromide; sodium hydride; triethylamine Yield given. Multistep reaction; | |
With ammonium hydroxide; trimethylsilyl bromide; sodium hydride; triethylamine Multistep reaction; |
bis(2-propyl)-p-toluenesulfonyloxymethylphosphonate
glycidyltrimethylammonium chloride
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
With ammonium hydroxide; sodium hydride Multistep reaction. Title compound not separated from byproducts; |
bis(2-propyl)-p-toluenesulfonyloxymethylphosphonate
glycidyltrimethylammonium chloride
N,N-dimethyl-formamide dimethyl acetal
Conditions | Yield |
---|---|
With sodium hydride Multistep reaction. Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
With 1.) CsCO3 1.) DMF, 120 deg C, 16 h, 2.) DMF, 20 deg C, 24 h; Multistep reaction. Title compound not separated from byproducts; |
Glycidyl trimethyl ammonium chloride(3033-77-0)'s molecular formula is C6H14NOCl and its formula weight is 151.6.
The density of glycidyl trimethyl ammonium chloride(3033-77-0) is 1.13 g/mL at 20 °C(lit.)
Its flash point is 170°C.
The molecular structure of glycidyl trimethyl ammonium chloride(3033-77-0):
1. | mmo-klp 2 mmol/L | MUREAV Mutation Research. 89 (1981),269. | ||
2. | cyt-rat:lvr 10 mg/L | MUREAV Mutation Research. 153 (1985),57. | ||
3. | scu-mus LD50:90 mg/kg | JCSOA9 Journal of the Chemical Society .(London, England.: )1947,176. |
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