616-30-8 | 3-Amino-1,2-propanediol

Packsize	Purity	Availability	Price	Discounted Price
25g	95%	in stock	$5.00	$4.00
100g	95%	in stock	$18.00	$13.00
500g	95%	in stock	$65.00	$46.00

Description

• Catalog Number: AB42758
• Chemical Name: 3-Amino-1,2-propanediol
• CAS Number: 616-30-8
• Molecular Formula: C3H9NO2
• Molecular Weight: 91.1091
• MDL Number: MFCD00008140
• SMILES: NCC(CO)O
• NSC Number: 67381

Computed Properties

• Complexity: 32
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 2
• Undefined Atom Stereocenter Count: 1
• XLogP3: -2

Upstream Synthesis Route

3-Amino-1,2-propanediol, also known as 3-Aminopropanediol or Serinol, is a versatile compound widely used in chemical synthesis. One of its key applications is as a building block in the production of pharmaceuticals, agrochemicals, and various specialty chemicals.In chemical synthesis, 3-Amino-1,2-propanediol serves as a valuable intermediate due to its unique chemical properties. It contains both amine and alcohol functional groups, making it a versatile starting material for the synthesis of a variety of compounds. The amine group allows for reactions with various electrophiles, while the alcohol group can undergo oxidation or esterification reactions.One common application of 3-Amino-1,2-propanediol is in the synthesis of biologically active molecules, where its structural features can play a crucial role in modulating the properties of the final compound. For example, it can be used in the preparation of beta-lactam antibiotics, anti-viral agents, and chiral ligands for asymmetric catalysis.Furthermore, 3-Amino-1,2-propanediol is utilized in the production of surfactants, polymers, and corrosion inhibitors. Its ability to participate in various chemical transformations makes it a valuable tool for organic chemists in designing and synthesizing new compounds for a wide range of applications.

Literature

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• Self-sorting chiral subcomponent rearrangement during crystallization.

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• Self-assembled monolayers with latent aldehydes for protein immobilization.

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• Chiral resolution of monosaccharides as 1-phenyl-3-methyl-5-pyrazolone derivatives by ligand-exchange CE using borate anion as a central ion of the chiral selector.

  Electrophoresis 20061201

• Chiral ligand exchange capillary electrophoresis using borate anion as a central ion.

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• A specific receptor site for glycerol, a new sweet tastant for Drosophila: structure-taste relationship of glycerol in the labellar sugar receptor cell.

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  Journal of agricultural and food chemistry 20031022

• Three new derivatives of 3-amino-1,2-propanediol; their spectral properties and biological evaluation.

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