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Home > Encyclopedia > Choline, hydroxide

Choline, hydroxide

pharmaceutical raw materials
Choline, hydroxide structure

Choline, hydroxide 

structure
  • CAS No:

    123-41-1

  • Formula:

    C5H14NO.HO

  • Chemical Name:

    Choline, hydroxide

  • 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

  • Categories:

    Organic Chemistry  >  Amides

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.

Choline, hydroxide Basic Attributes

121.18

121.110275

204-625-1

7THJ3EG9SY

DTXSID9047467

2923900090

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

Methods of 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-

Uses

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

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

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