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100869-07-6

2-AMINOMETHYL-4-METHYL-PENTANOIC ACID, also known as L-valine, is a non-proteinogenic amino acid derivative with the molecular formula C8H17NO2. It is an essential amino acid that cannot be synthesized by the body and must be obtained from the diet. L-valine plays a vital role in promoting muscle growth, tissue repair, and immune function, making it a significant component in sports nutrition, dietary supplements, and potentially beneficial for individuals with liver and gallbladder disorders.

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  • 100869-07-6 Structure

  • Basic information

    1. Product Name: 2-AMINOMETHYL-4-METHYL-PENTANOIC ACID
    2. Synonyms: 2-AMINOMETHYL-4-METHYL-PENTANOIC ACID;RARECHEM AK HP A094;2-(Aminomethyl)-4-methyl-pentanoic acid HCl
    3. CAS NO:100869-07-6
    4. Molecular Formula: C7H15NO2
    5. Molecular Weight: 145.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100869-07-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 249.115 °C at 760 mmHg
    3. Flash Point: 104.461 °C
    4. Appearance: /
    5. Density: 1.014 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.51±0.21(Predicted)
    10. CAS DataBase Reference: 2-AMINOMETHYL-4-METHYL-PENTANOIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-AMINOMETHYL-4-METHYL-PENTANOIC ACID(100869-07-6)
    12. EPA Substance Registry System: 2-AMINOMETHYL-4-METHYL-PENTANOIC ACID(100869-07-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 100869-07-6(Hazardous Substances Data)

100869-07-6 Usage

Uses

Used in Sports Nutrition and Dietary Supplements:
2-AMINOMETHYL-4-METHYL-PENTANOIC ACID is used as a nutritional supplement for promoting muscle growth and tissue repair. As an essential amino acid, it supports the body's protein synthesis and helps athletes and individuals engaged in regular physical activity to recover more effectively from exercise-induced muscle damage.
Used in Immune Function Enhancement:
2-AMINOMETHYL-4-METHYL-PENTANOIC ACID is used as an immune-boosting agent to support the body's immune system. Its role in immune function may offer potential benefits for individuals with compromised immune systems or those seeking to improve their overall health and well-being.
Used in Liver and Gallbladder Health:
2-AMINOMETHYL-4-METHYL-PENTANOIC ACID is used as a supportive agent for liver and gallbladder health. Its potential benefits for individuals with liver and gallbladder disorders make it a valuable component in dietary supplements and health products aimed at maintaining liver and gallbladder function.
Used in Pharmaceutical and Biomedical Research:
2-AMINOMETHYL-4-METHYL-PENTANOIC ACID, as a non-proteinogenic amino acid, is used in pharmaceutical and biomedical research for the development of new drugs and therapies. Its unique properties and functions may contribute to the discovery of novel treatments for various health conditions and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 100869-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100869-07:
(8*1)+(7*0)+(6*0)+(5*8)+(4*6)+(3*9)+(2*0)+(1*7)=106
106 % 10 = 6
So 100869-07-6 is a valid CAS Registry Number.

100869-07-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(aminomethyl)-4-methylpentanoic acid

1.2 Other means of identification

Product number -
Other names 3-Amino-2-isobutyl-propionsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100869-07-6 SDS

100869-07-6Relevant articles and documents

Evaluation of several routes to advanced pregabalin intermediates: Synthesis and enantioselective enzymatic reduction using ene-reductases

Debarge, Sebastien,McDaid, Paul,O'Neill, Pat,Frahill, James,Wong, John W.,Carr, Donncha,Burrell, Adam,Davies, Simon,Karmilowicz, Mike,Steflik, Jeremy

, p. 109 - 121 (2014)

This publication describes the evaluation of four synthetic routes to the advanced pregabalin (Lyrica) intermediate 7. Asymmetric reduction of (E)-7 with an ene-reductase (OPR1 from Lycopersicon esculentum) gave a saturated cyanoester intermediate 5 with the desired S stereocenter in ≥99% ee. OPR1 also catalyzed the reduction of (Z)-7 to (S)-5, but with lower conversion and selectivity.

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