Product Name:(R)-3-aminobutan-1-ol

IUPAC Name:(3R)-3-aminobutan-1-ol

CAS:61477-40-5
Molecular Formula:C4H11NO
Purity:97%
Catalog Number:CM108315
Molecular Weight:89.14

Packing Unit Available Stock Price($) Quantity
CM108315-100g in stock ƋɅ
CM108315-500g in stock ƻƙƋ

For R&D use only.

Inquiry Form

   refresh    

Product Details

CAS NO:61477-40-5
Molecular Formula:C4H11NO
Melting Point:-
Smiles Code:C[C@@H](N)CCO
Density:
Catalog Number:CM108315
Molecular Weight:89.14
Boiling Point:168°C at 760 mmHg
MDL No:MFCD13184351
Storage:Keep in dark place, store at 2-8°C.

Category Infos

Aliphatic Chain Compounds
Aliphatic chain compounds include aliphatic compounds and chain compounds containing other elements or groups. Aliphatic hydrocarbons are hydrocarbons with the basic properties of aliphatic compounds. In aliphatic compounds, carbon atoms are arranged in straight chain, branched chain or cyclic, which are respectively called straight chain aliphatic hydrocarbons, branched chain aliphatic hydrocarbons and alicyclic hydrocarbons. Some cyclic hydrocarbons are different in nature from aromatic hydrocarbons, and are very similar to aliphatic hydrocarbons. Such cyclic hydrocarbons are called alicyclic hydrocarbons. In this way, aliphatic hydrocarbons become a general term for all hydrocarbons except aromatic hydrocarbons. Aliphatic hydrocarbons and their derivatives (including halogenated hydrocarbons) and alicyclic hydrocarbons and their derivatives are collectively referred to as aliphatic compounds.

Column Infos

Alcohols
Alcohol is a type of organic compound that carries at least one hydroxyl ( −OH) functional group bound to a saturated carbon atom.

Related Products



Product Other Information

Product Overview (R)-3-aminobutan-1-ol, also known as (R)-1-amino-3-butyrolactam, is an organic compound that is commonly used in scientific research. It is a colorless liquid with a faint odor, and it is soluble in water and other organic solvents. As a chiral molecule, (R)-3-aminobutan-1-ol has two enantiomers, (R)- and (S)-, which differ in their physical and chemical properties. (R)-3-aminobutan-1-ol has a variety of applications in scientific research, including synthesis, catalysis, and drug discovery.
Synthesis and Application (R)-3-aminobutan-1-ol can be synthesized through a variety of methods, including chemical synthesis, enzymatic synthesis, and biotransformation. In chemical synthesis, (R)-3-aminobutan-1-ol can be synthesized from (R)-3-aminobutanol and a base, such as sodium hydroxide. In enzymatic synthesis, (R)-3-aminobutan-1-ol can be synthesized from (R)-3-aminobutanol and an enzyme, such as a lipase or esterase. In biotransformation, (R)-3-aminobutan-1-ol can be synthesized from (R)-3-aminobutanol and a microorganism, such as a bacterium or fungus. (R)-3-aminobutan-1-ol has a variety of applications in scientific research, including synthesis, catalysis, and drug discovery. In synthesis, (R)-3-aminobutan-1-ol is used as a starting material in the synthesis of various compounds, including drugs, dyes, and polymers. In catalysis, (R)-3-aminobutan-1-ol is used as a catalyst in the synthesis of various compounds, including pharmaceuticals, agrochemicals, and fragrances. In drug discovery, (R)-3-aminobutan-1-ol is used as a starting material in the synthesis of various drugs, including antibiotics, anti-cancer drugs, and anti-inflammatory drugs.
Future Directions The future directions of (R)-3-aminobutan-1-ol research include further exploration of its biochemical and physiological effects, further exploration of its mechanism of action, further exploration of its use in drug discovery, and further exploration of its use in the synthesis of various compounds. In addition, further research is needed to determine the safety and efficacy of (R)-3-aminobutan-1-ol in humans.