Home >Organic Chemicals > 3-Aminobutane-1,2,4-triol
- Chemical Name: 3-Aminobutane-1,2,4-triol
- CAS No.: 83168-64-3
Factory supply good quality 3-Aminobutane-1,2,4-triol 83168-64-3 with stock
- Molecular Formula: C4H11NO3
- Molecular Weight: 121.136
- Vapor Pressure: 1.57E-06mmHg at 25°C
- Refractive Index: 1.538
- Boiling Point: 357 °C at 760 mmHg
- Flash Point: 169.7 °C
- PSA： 86.71000
- Density: 1.323g/cm3
- LogP: -1.64050
3-Aminobutane-1,2,4-triol(Cas 83168-64-3) Usage
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General Description |
3-Aminobutane-1,2,4-triol, also known as 2-Amino-2-methyl-1,3-propanediol, is a chemical compound with the molecular formula C4H11NO3. It is a colorless, odorless, and hygroscopic solid that is soluble in water, alcohol, and polar organic solvents. 3-Aminobutane-1,2,4-triol is primarily used as a component in the synthesis of pharmaceuticals, such as the antiviral drug Zanamivir. It also has applications in the production of corrosion inhibitors, surfactants, and chelating agents. Additionally, it can act as a stabilizer in certain cosmetic and personal care products. The compound has low acute oral toxicity and is considered to be relatively safe for use in various industrial and consumer applications. |
InChI:InChI=1/C4H11NO3/c5-3(1-6)4(8)2-7/h3-4,6-8H,1-2,5H2
83168-64-3 Relevant articles
Characterization of a novel amine transaminase from Halomonas elongata
Cerioli, Lorenzo,Planchestainer, Matteo,Cassidy, Jennifer,Tessaro, Davide,Paradisi, Francesca
, p. 141 - 150 (2015/09/01)
Chiral amines are indispensable building...
Preparation of enantioenriched tetraols and triolamines from a common epoxide
Kaviani-Joupari, Makan,Schramm, Michael P.
, p. 5014 - 5017 (2013/09/02)
We identify a silylcyclopentene oxide th...
A toolbox approach for the rapid evaluation of multi-step enzymatic syntheses comprising a 'mix and match' E. coli expression system with microscale experimentation
Rios-Solis,Halim,Cazares,Morris,Ward,Hailes,Dalby,Baganz,Lye
scheme or table, p. 192 - 203 (2012/04/18)
This work describes an experimental 'too...
2,6-disubstituted derivatives of 3-nitropyrazines useful as adjuncts to radiation therapy
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, (2008/06/13)
2,6-Disubstituted derivatives of 3-nitro...
83168-64-3 Process route
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83168-64-3
2-amino-hydroxymethyl-1,3-propanediol
| Conditions | Yield |
|---|---|
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533-50-6
L-erythrulose
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62397-88-0,83168-64-3,87069-32-7,111453-48-6,111554-89-3
(2S,3R)-2-amino-1,3,4-butanetriol
| Conditions | Yield |
|---|---|
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With
transaminase; pyridoxal 5'-phosphate; isopropylamine;
aq. buffer;
Enzymatic reaction;
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|
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With
(S)-1-phenyl-ethylamine; Halomonas elongata ω-transaminase;
In
aq. phosphate buffer;
at 37 ℃;
pH=8;
Enzymatic reaction;
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83168-64-3 Upstream products
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82953-44-4
N-[(2R,3S,4R,5S,6R)-3-Acetylamino-2-((1R,2S)-2-acetylamino-3-hydroxy-1-hydroxymethyl-propoxy)-5-((2R,3S,4R,5S,6R)-3,4-bis-acetylamino-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-4-yl]-acetamide
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533-50-6
L-erythrulose
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1450667-18-1
C16 H19 NOSi