Pentanoic acid, 3-amino-4-methyl-, (3R)-
(3R)-3-Amino-4-methylpentanoic acid
CAS: 5699-54-7;75992-50-6
Molecular Formula: C6H13NO2
Pentanoic acid, 3-amino-4-methyl-, (3R)- - Names and Identifiers
| Name | (3R)-3-Amino-4-methylpentanoic acid |
| Synonyms | D-β-Hoval-OH L-BETA-LEUCINE (R)-Homo-Beta-Valine (R)-HOMO-BETA-VALINE (3R)-3-Amino-4-methylpentanoic acid Pentanoic acid, 3-amino-4-methyl-, (3R)- |
| CAS | 5699-54-7 75992-50-6 |
| InChI | InChI=1/C6H13NO2/c1-4(2)5(7)3-6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t5-/m1/s1 |
Pentanoic acid, 3-amino-4-methyl-, (3R)- - Physico-chemical Properties
| Molecular Formula | C6H13NO2 |
| Molar Mass | 131.17 |
| Density | 1.035±0.06 g/cm3(Predicted) |
| Melting Point | 206℃ |
| Boling Point | 232.0±23.0 °C(Predicted) |
| Flash Point | 94.1°C |
| Vapor Presure | 0.0212mmHg at 25°C |
| pKa | 3.81±0.10(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
| Refractive Index | 1.462 |
| MDL | MFCD00800505 |
Pentanoic acid, 3-amino-4-methyl-, (3R)- - Introduction
(3R)-3-Amino-4-methylpentanoic acid((R)-beta-leucine) is also known as (3R)-3-amino-4-methylpentanoic acid((3R)-3-Amino-4-methylpentanoic acid). The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
- (3R)-3-Amino-4-methylpentanoic acid is an organic compound with a chemical formula of C6H13NO2 and a molecular weight of 131.17g/mol.
-It is colorless crystals, insoluble in water, soluble in organic solvents such as ethanol and dichloromethane.
-It has a chiral center, so there are two enantiomers:(R)-and (S)-.
Use:
- (3R)-3-Amino-4-methylpentanoic acid is an important chiral amino acid, which is widely used in pharmaceutical and biochemical research.
-It can be used as a chiral reference compound in protein expression and structural analysis, as well as a chiral source in the synthesis of chiral drugs.
-The compound can also be used for the synthesis of chiral ligands and catalysts, as well as the study of biologically active molecules.
Preparation Method:
- (3R)-3-Amino-4-methylpentanoic acid is usually obtained by chemical synthesis.
-One preparation method is to convert the chiral precursor into (3R)-3-Amino-4-methylpentanoic acid by chiral synthesis.
-This method usually involves the steps of catalytic hydrogenation reduction of chiral compounds, stereoselective amination reactions, or selective separation of chiral synthesis intermediates.
Security Information:
- (3R)-3-Amino-4-methylpentanoic acid is relatively safe for the human body under general conditions.
-However, as an organic compound, it is still necessary to pay attention to general laboratory safety practices when using it to avoid skin contact, inhalation or ingestion.
-During storage and handling, it should be kept dry and sealed to avoid contact with oxidants and strong acids.
Please note that for specific uses and preparation methods, it is best to consult relevant professionals and follow relevant regulations and guidance.
Nature:
- (3R)-3-Amino-4-methylpentanoic acid is an organic compound with a chemical formula of C6H13NO2 and a molecular weight of 131.17g/mol.
-It is colorless crystals, insoluble in water, soluble in organic solvents such as ethanol and dichloromethane.
-It has a chiral center, so there are two enantiomers:(R)-and (S)-.
Use:
- (3R)-3-Amino-4-methylpentanoic acid is an important chiral amino acid, which is widely used in pharmaceutical and biochemical research.
-It can be used as a chiral reference compound in protein expression and structural analysis, as well as a chiral source in the synthesis of chiral drugs.
-The compound can also be used for the synthesis of chiral ligands and catalysts, as well as the study of biologically active molecules.
Preparation Method:
- (3R)-3-Amino-4-methylpentanoic acid is usually obtained by chemical synthesis.
-One preparation method is to convert the chiral precursor into (3R)-3-Amino-4-methylpentanoic acid by chiral synthesis.
-This method usually involves the steps of catalytic hydrogenation reduction of chiral compounds, stereoselective amination reactions, or selective separation of chiral synthesis intermediates.
Security Information:
- (3R)-3-Amino-4-methylpentanoic acid is relatively safe for the human body under general conditions.
-However, as an organic compound, it is still necessary to pay attention to general laboratory safety practices when using it to avoid skin contact, inhalation or ingestion.
-During storage and handling, it should be kept dry and sealed to avoid contact with oxidants and strong acids.
Please note that for specific uses and preparation methods, it is best to consult relevant professionals and follow relevant regulations and guidance.
Last Update：2024-04-09 20:49:11
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Multiple Specifications
Product Name: DL-β-Leucine Visit Supplier Webpage Request for quotationCAS: 5699-54-7
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Multiple Specifications
Product Name: DL-β-Leucine Visit Supplier Webpage Request for quotationCAS: 5699-54-7
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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