CAS 5856-63-3

(R)-2-Amino-1-butanol

Description:

(R)-2-Amino-1-butanol, with the CAS number 5856-63-3, is an organic compound characterized by its amino alcohol structure. It features a primary amine group (-NH2) and a hydroxyl group (-OH) attached to a four-carbon butane chain, specifically at the second carbon, which imparts chirality to the molecule. This compound is typically a colorless to pale yellow liquid and is soluble in water due to the presence of both the amine and alcohol functional groups, which can engage in hydrogen bonding. Its chiral nature allows it to exist in two enantiomeric forms, with the (R)-configuration being one of them, which can exhibit different biological activities compared to its (S)-counterpart. (R)-2-Amino-1-butanol is utilized in various applications, including as a building block in organic synthesis, in pharmaceuticals, and as a potential chiral auxiliary in asymmetric synthesis. Its properties make it of interest in both industrial and research settings, particularly in the development of chiral drugs and compounds.

Formula: C₄H₁₁NO

InChI: InChI=1S/C4H11NO/c1-2-4(5)3-6/h4,6H,2-3,5H2,1H3/t4-/m1/s1

InChI key: InChIKey=JCBPETKZIGVZRE-SCSAIBSYSA-N

SMILES: [C@@H](CC)(CO)N

Synonyms:

• (-)-2-Amino-1-butanol
• (2R)-1-hydroxybutan-2-aminium
• (2R)-2-Amino-1-butanol
• (2R)-2-Aminobutan-1-ol
• (R)-(-)-2-Aminobutan-1-ol
• (R)-2-Aminobutanol
• 1-Butanol, 2-amino-, (-)-
• 1-Butanol, 2-amino-, (2R)-
• 1-Butanol, 2-amino-, (R)-
• 1-Butanol, 2-amino-, l-
• 2-Aminobutanol
• 2R-Aminobutanol
• <span class="text-smallcaps">D</span>-(-)-2-Amino-1-butanol
• D(+)-2-Amino-1-butanol
• D-(+)-2-Amino butanol
• D-(+)-Amino butanol
• D-2-aminobutanol
• D-Amino-1-butanol
• L-2-Amino-1-butanol
• L-2-aminobutanol
• L-Amino-1-butanol
• [(R)-1-(Hydroxymethyl)propyl]amine
• R(-)-2-Amino-1-Butanol

(R)-(-)-2-Amino-1-butanol

CAS: 5856-63-3

Formula: C₄H₁₁NO

Purity: >94.0%(GC)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 89.14

Ref: 3B-A0972

(R)-(-)-2-Amino-1-butanol, 98%

CAS: 5856-63-3

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₄H₁₁NO

Purity: 98%

Color and Shape: Clear colorless to pale yellow, Liquid or viscous liquid

Molecular weight: 89.14

Ref: 02-B25212

(R)-(-)-2-Amino-1-Butanol

CAS: 5856-63-3

Formula: C₄H₁₁NO

Purity: 98%

Color and Shape: Liquid

Molecular weight: 89.1362

Ref: IN-DA0032DH

R-(-)-2-Amino-1-butanol

CAS: 5856-63-3

Formula: C₄H₁₁NO

Molecular weight: 89.14

Ref: 7W-GK5394

(R)-(-)-2-Aminobutan-1-ol

CAS: 5856-63-3

(R)-(-)-2-Aminobutan-1-ol

Formula: C₄H₁₁NO

Purity: 98%

Color and Shape: clear colourless liquid

Molecular weight: 89.14g/mol

Ref: 54-OR5871

(R)-(-)-2-Amino-1-butanol

Controlled Product

CAS: 5856-63-3

Applications (R)-(-)-2-Amino-1-butanol (cas# 5856-63-3) is a useful research chemical.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Formula: C₄H₁₁NO

Color and Shape: Neat

Molecular weight: 89.14

Ref: TR-A602205

(R)-(-)-2-Amino-1-butanol

CAS: 5856-63-3

Formula: C₄H₁₁NO

Purity: 98%

Color and Shape: Liquid

Molecular weight: 89.138

Ref: 10-F012703

(R)-(-)-2-Amino-1-butanol

CAS: 5856-63-3

(R)-(-)-2-Amino-1-butanol is an organic compound that is used as a reagent in the synthesis of pharmaceuticals. It has antimycobacterial properties and can be used to treat tuberculosis. The mechanism for its antimycobacterial activity is not fully understood, but it may involve copper complex formation with the mycobacteria. The chloride ion may also play a role in this process by binding to the copper complex and increasing its solubility in water. This compound may react with aminothiols from the host cell, leading to degradation of DNA, RNA, and proteins. (R)-(-)-2-Amino-1-butanol has been shown to have cytotoxic effects on colorectal adenocarcinoma cells and human lung cancer cells in culture. It also inhibits human colon carcinoma cells in culture through the production of organic acids such as formic acid and acetic acid.

Formula: C₄H₁₁NO

Purity: Min. 95%

Molecular weight: 89.14 g/mol

Ref: 3D-FA60173