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2002-24-6

2002-24-6 Structure

2002-24-6 Structure
IdentificationMore
[Name]

ETHANOLAMINE HYDROCHLORIDE
[CAS]

2002-24-6
[Synonyms]

2-AMINOETHANOL HYDROCHLORIDE
2-HYDROXYETHYLAMINE HYDROCHLORIDE
2-HYDROXYETHYLAMMONIUM CHLORIDE
ETHANOLAMINE HCL
ETHANOLAMINE HYDROCHLORIDE
ETHANOLAMMONIUM CHLORIDE
MONOETHANOLAMINE HCL
MONOETHANOLAMINE HYDROCHLORIDE
2-amino-ethanohydrochloride
beta-aminoethanolhydrochloride
colaminehydrochloride
Ethanol,2-amino-,hydrochloride
ethanolaminechloride
meahydrochloride
ETHANOLAMINE HYDROCHLORIDE, 98+%
ETHANOLAMINE HYDROCHLORIDE, 99+%
ETHANOL-13C2-AMINE.HCL 99%
2-AminoethanolHCl=2-HydroxyethylamineHCl
Hydroxyethylamine hydrochloride
2-aminoethanol-13c2hydrochloride
[EINECS(EC#)]

217-900-6
[Molecular Formula]

C2H8ClNO
[MDL Number]

MFCD00012892
[Molecular Weight]

97.54
[MOL File]

2002-24-6.mol
Chemical PropertiesBack Directory
[Appearance]

White or slightly beige agglomerating crystals
[Melting point ]

82-84 °C(lit.)
[density ]

1.07g/cm3 at 20—25°C
1.12g/cm3 at 20—25°C
[storage temp. ]

Store at RT.
[solubility ]

DMSO (Slightly, Heated)
[form ]

Agglomerating Crystals
[color ]

White or slightly beige
[Specific Gravity]

1.146
[Odor]

Odorless
[PH]

9—10
[pka]

9.5(at 25℃)
[Water Solubility ]

almost transparency
[Sensitive ]

Hygroscopic
[Merck ]

14,3727
[BRN ]

3542892
[Stability:]

Hygroscopic
[Cosmetics Ingredients Functions]

BUFFERING
[InChI]

1S/C2H7NO.ClH/c3-1-2-4;/h4H,1-3H2;1H
[InChIKey]

PMUNIMVZCACZBB-UHFFFAOYSA-N
[SMILES]

NCCO.[H]Cl
[LogP]

-1.308 (est)
[CAS DataBase Reference]

2002-24-6(CAS DataBase Reference)
[EPA Substance Registry System]

Ethanol, 2-amino-, hydrochloride (2002-24-6)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338-P280a-P304+P340-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[WGK Germany ]

1
[RTECS ]

KJ6370000
[F ]

3-10
[TSCA ]

Yes
[HS Code ]

29221100
[Storage Class]

11 - Combustible Solids
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Monoethanolamine-->Water-->Hydrochloric acid
[Preparation Products]

Piperazine-->N-(2-Hydroxyethyl)glycine-->Ethanamine, 2-(triphenylmethoxy)-
Hazard InformationBack Directory
[Chemical Properties]

White or slightly beige agglomerating crystals
[Uses]

Ethanolamine hydrochloride has been used:
  • in overnight incubation of the tips to attach primary amine groups at the tip surface
  • in the preparation of DMEM (dulbecco′s modified eagle′s medium)/F-12 media to culture human epidermal growth factor receptor 2 (HER2) cells derived from MMTV-HER2 transgenic mouse mammary tumors
  • to administer the cultures to study its effect on the endogenous phosphatidyl ethanolamine pool and autophagy process

[Biochem/physiol Actions]

Ethanolamine hydrochloride is utilized as a carbon and nitrogen source by bacteria that differs phylogenetically. It exists as phosphotidylethanolamine in the bacterial and mammalian cell membrane. Ethanolamine-ammonia lyase is responsible for the degradation of ethanolamine into acetaldehyde and ammonia. Ethanolamine is known to positively support lipid accumulation in photosynthetic organism model.
[Synthesis]

Monoethanolamine

141-43-5

ETHANOLAMINE HYDROCHLORIDE

2002-24-6

General procedure for the synthesis of ethanolamine hydrochloride from 2-aminoethanol: Reagents and reaction conditions: 36% concentrated hydrochloric acid, room temperature. Operating steps: 1. 15.0 g of 2-aminoethanol was weighed and added to three reaction flasks. 2. 27.0 g of 36% concentrated hydrochloric acid was added dropwise at a constant rate through a dropping funnel under stirring conditions, and the reaction temperature was controlled to be no more than 40 °C. 3. 3. after completion of the dropwise addition, the reaction mixture was continued to be stirred for 20 minutes until the pH was about 2 and the reaction was terminated. 4. remove water from the reaction system by concentration under reduced pressure until a very small amount of water remains. 5. A small amount of toluene was added and the residual water was further removed by azeotropic distillation. 6. The reaction mixture was rapidly cooled to give 23.7 g of a slightly light brown solid product, ethanolamine hydrochloride (M-07), in 99% yield.

[Purification Methods]

Recrystallise the salt from EtOH. It is deliquescent; store it dry. [Beilstein 4 IV 1406.]
[References]

[1] Bulletin des Societes Chimiques Belges, 1984, vol. 93, # 10, p. 903 - 912
[2] Patent: CN105585607, 2016, A. Location in patent: Paragraph 0107; 0108; 0109; 0110
[3] Green Chemistry, 2016, vol. 18, # 9, p. 2834 - 2842
[4] Green Chemistry, 2017, vol. 19, # 13, p. 3152 - 3163
Spectrum DetailBack Directory
[Spectrum Detail]

ETHANOLAMINE HYDROCHLORIDE(2002-24-6)1HNMR
ETHANOLAMINE HYDROCHLORIDE(2002-24-6)13CNMR
ETHANOLAMINE HYDROCHLORIDE(2002-24-6)IR1
ETHANOLAMINE HYDROCHLORIDE(2002-24-6)IR2
ETHANOLAMINE HYDROCHLORIDE(2002-24-6)IR3
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Ethanolamine hydrochloride, 99+%(2002-24-6)
[Alfa Aesar]

Ethanolamine hydrochloride, 98+%(2002-24-6)
[Sigma Aldrich]

2002-24-6(sigmaaldrich)
[TCI AMERICA]

Ethanolamine Hydrochloride,>98.0%(T)(2002-24-6)
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