Choline, hydroxide
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Choline, hydroxide
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CAS No:
123-41-1
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Formula:
C5H14NO.HO
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Chemical Name:
Choline, hydroxide
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Synonyms:
Ethanaminium,2-hydroxy-N,N,N-trimethyl-,hydroxide (1:1);Choline,hydroxide;Ethanaminium,2-hydroxy-N,N,N-trimethyl-,hydroxide;Bursine;Fagine;Gossypine;(β-Hydroxyethyl)trimethylammonium hydroxide;Luridine;Sincaline;Sinkalin;Sinkaline;Vidine;(2-Hydroxyethyl)trimethylammonium hydroxide;Trimethyl(hydroxyethyl)ammonium hydroxide;Trimethyl(2-hydroxyethyl)ammonium hydroxide;N,N,N-Trimethyl-N-(2-hydroxyethyl)ammonium hydroxide;Cholinium hydroxide;N,N,N-Trimethyl-N-hydroxyethylammonium hydroxide;2-Hydroxy-N,N,N-trimethylethanaminium hydroxide;259229-71-5
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CAS No:
Description
Withheld
A basic constituent of lecithin that is found in many plants and animal organs. It is important as a precursor of acetylcholine, as a methyl donor in various metabolic processes, and in lipid metabolism.
Characteristics
21.2
-0.49190
White Granular Powder
1.09 g/mL at 20 °C
92 °F
n20/D 1.4304
Micible with water.
2-8°C
Safety Information
II
8
UN 3286 3/PG 2
1
34-35-43-39/23/24/25-23/24/25-10-R35
26-36/37/39-45-S45-S36/37/39-S26
GA4025500
C,T
Stable. Combustible. Incompatible with strong oxidizing agents.
P260, P261, P264, P270, P271, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P314, P321, P363, P403+P233, P405, P501
H314
|Danger|H314 (99.67%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P261, P264, P270, P271, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P314, P321, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 303 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Endogenous factors or drugs that increase the transport and metabolism of LIPIDS including the synthesis of LIPOPROTEINS by the LIVER and their uptake by extrahepatic tissues. (See all compounds classified as Lipotropic Agents.)|Drugs used to specifically facilitate learning or memory, particularly to prevent the cognitive deficits associated with dementias. These drugs act by a variety of mechanisms. (See all compounds classified as Nootropic Agents.)
2-Hydroxy-N,N,N-trimethylethanaminium
Choline, hydroxide Use and Manufacturing
The ethanol solution of trimethylamine is added to the reaction pot, ethylene oxide is introduced at about 30°C, and the product is obtained by stirring and reacting for 4 hours. (CH3)3N+(CH2CH2)O+H20→[(CH3)3N+CH2CH2OH]OH-
Used as a biochemical reagent
Plating agents and surface treating agents
Electrical and electronic products
Computer and electronic product manufacturing|Ethanaminium, 2-hydroxy-N,N,N-trimethyl-, hydroxide (1:1): ACTIVE
Computed Properties
Molecular Weight:121.18
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:121.110278721
Monoisotopic Mass:121.110278721
Topological Polar Surface Area:21.2
Heavy Atom Count:8
Complexity:46.5
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Participate in the normal physiological functions of the human body
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