132605-98-2

Basic information

• Product Name: (R)-3-AMino-2-Methylpropanoic acid-HCl
• Synonyms: (R)-3-AMino-2-Methylpropanoic acid-HCl;(R)-3-AMino-2-Methylpropanoic acid hydrochloride
• CAS NO: 132605-98-2
• Molecular Formula: C4H10ClNO2
• Molecular Weight: 139.5807
• Mol File: 132605-98-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: (R)-3-AMino-2-Methylpropanoic acid-HCl(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-AMino-2-Methylpropanoic acid-HCl(132605-98-2)
• EPA Substance Registry System: (R)-3-AMino-2-Methylpropanoic acid-HCl(132605-98-2)

Safety Data

• Hazardous Substances Data: 132605-98-2(Hazardous Substances Data)

Usage

General Description

(R)-3-Amino-2-methylpropanoic acid-HCl, also known as l-isoleucine hydrochloride, is a chemical compound with the molecular formula C6H14ClNO2. It is the hydrochloride salt of l-isoleucine, one of the essential amino acids. (R)-3-AMino-2-Methylpropanoic acid-HCl plays a critical role in protein synthesis and is found in high concentrations in muscle tissue. It is also used as a nutritional supplement and is commonly found in various dietary and sports nutrition products. The hydrochloride form of l-isoleucine is often used in pharmaceuticals and research applications due to its enhanced stability and solubility in water. Overall, l-isoleucine hydrochloride is an important biochemical that is essential for the proper functioning of the human body.

Upstream product

• 22560-81-2 ethyl 3-amino-2-methylpropanoate 
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Relevant articles and documents

An Efficient Two-Step Preparation of α-, β-, γ- or δ-Amino Acids from 2-Pyrazinones, 2-Hydroxypyrimidines or 2-Pyridones Respectively

A practical and efficient two-step procedure is reported for the preparation of a variety of α-, β-, γ- and δ-amino acids from 2-pyridone, 2-pyrazinone or 2-hydroxypyrimidine and derivatives. The procedure is amenable to scale-up and in most cases no chromatographic purification of the product is required. This approach is useful, especially in the synthesis of amino acids or deuterated amino acids that are not obtained by other methods.

The Stereochemistry of Organometallic Compounds. XXXII. Hydrocyanation of Derivatives of Amino Alkynes

The hydrocyanation of a range of amino alkyne derivatives has been studied by using nickel-based catalyst systems.The phthalimido derivatives have been shown to give good yields of unsaturated cyano amine derivatives, and some of these have been converted into both saturated and unsaturated amino acids.