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3-((2-HYDROXYETHYL)AMINO)-1-PROPANOL

  • CAS: 19344-29-7
  • Purity: 99%
  • 3-((2-HYDROXYETHYL)AMINO)-1-PROPANOL 19344-29-7 with purity >99% Low price in stock
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3-((2-HYDROXYETHYL)AMINO)-1-PROPANOL 19344-29-7 with purity >99% Low price in stock

  • Molecular Formula: C5H13 N O2
  • Molecular Weight: 119.164
  • Vapor Pressure: 0.0019mmHg at 25°C 
  • Boiling Point: 259.4°Cat760mmHg 
  • Flash Point: 137.9°C 
  • PSA: 52.49000 
  • Density: 1.037g/cm3 
  • LogP: -0.65840 

3-((2-HYDROXYETHYL)AMINO)-1-PROPANOL(Cas 19344-29-7) Usage

General Description

3-((2-Hydroxyethyl)Amino)-1-Propanol is a chemical compound that belongs to the class of organic compounds known as aminoalcohols, which are alcohols that contain an amino group. It is typically used in a variety of industrial and scientific applications. The hydroxyethyl group and the amino group in the structure make it a dual functional compound. Such compounds are often used as intermediates in organic synthesis due to their reactivity. Moreover, the presence of these functional groups endows the compound with polar properties, which might make it soluble in water and other polar solvents. However, like other chemicals, it should be handled with care as exposure may cause various health risks.

InChI:InChI=1/C5H13NO2/c7-4-1-2-6-3-5-8/h6-8H,1-5H2

19344-29-7 Relevant articles

Compounds having a plurality of nitrogenous substitutents

-

, (2008/06/13)

Novel compounds having the formula: STR1...

SUBSTITUTED HETEROCYCLIC COMPOUNDS

-

, (2008/06/13)

Novel compounds having the formula: STR1...

Nitrogenous macrocyclic compounds

-

, (2011/08/10)

PCT No. PCT/US96/04215 Sec. 371 Date Sep...

Candida antarctica Lipase-Catalyzed Monoaminolysis of Diesters with Aminoalcohols. Chemoenzymatic Synthesis of Macrocycles and Aminodiols

Quiros, Margarita,Rebolledo, Francisca,Gotor, Vicente

, p. 1917 - 1934 (2007/10/02)

Candida antarctica lipase catalyzes the ...

19344-29-7 Process route

methyl 2-(2-hydroxyethylcarbamoyl)ethanoate

methyl 2-(2-hydroxyethylcarbamoyl)ethanoate

3-[(2-hydroxyethyl)amino]propanol
19344-29-7

3-[(2-hydroxyethyl)amino]propanol

Conditions
Conditions Yield
With lithium aluminium tetrahydride; In 1,4-dioxane; for 24h; Heating;
90%
oxirane
75-21-8,99932-75-9

oxirane

propan-1-ol-3-amine
156-87-6

propan-1-ol-3-amine

3-[(2-hydroxyethyl)amino]propanol
19344-29-7

3-[(2-hydroxyethyl)amino]propanol

Conditions
Conditions Yield
With ethanol; at 100 ℃;

19344-29-7 Upstream products

  • 75-21-8
    75-21-8

    oxirane

  • 156-87-6
    156-87-6

    propan-1-ol-3-amine

19344-29-7 Downstream products

  • 42453-19-0
    42453-19-0

    N- <2-chlor-ethyl> -3-chlor-propylamin

  • 6965-77-1
    6965-77-1

    N-(2-hydroxyethyl)-N-(3-hydroxypropyl)-para-toluenesulfonamide

  • 121335-74-8
    121335-74-8

    7-tosylperhydro-1,3,6-dioxazonine

  • 23207-87-6
    23207-87-6

    N- <2-chlor-aethyl> -N- <3-chlor-propyl> -benzylamin

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