D-VALINE METHYL ESTER HYDROCHLORIDE

98%

Reagent Code: #76396
label
Alias D-Valine Methyl Ester Hydrochloride D-Valine Methyl Ester
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CAS Number 21685-47-2

science Other reagents with same CAS 21685-47-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.63 g/mol
Formula C₆H₁₄ClNO₂
badge Registry Numbers
EC Number 230-454-7
thermostat Physical Properties
Melting Point ~170 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in the synthesis of peptides and as a chiral building block in organic chemistry. It serves as a key intermediate in the production of pharmaceuticals, particularly in the development of drugs that require specific stereochemistry for enhanced efficacy. Commonly employed in research laboratories for studying enzyme-substrate interactions and in the preparation of modified amino acids for biochemical studies. Its stability and solubility make it suitable for various chemical reactions, including esterification and amidation processes.

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Test Parameter Specification
Purity 98-100%
Appearance Crystalline powder
Melting Point 170

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿520.00
inventory 5g
10-20 days ฿1,150.00
inventory 25g
10-20 days ฿2,910.00
inventory 100g
10-20 days ฿9,720.00

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D-VALINE METHYL ESTER HYDROCHLORIDE
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Used primarily in the synthesis of peptides and as a chiral building block in organic chemistry. It serves as a key intermediate in the production of pharmaceuticals, particularly in the development of drugs that require specific stereochemistry for enhanced efficacy. Commonly employed in research laboratories for studying enzyme-substrate interactions and in the preparation of modified amino acids for biochemical studies. Its stability and solubility make it suitable for various chemical reactions, incl

Used primarily in the synthesis of peptides and as a chiral building block in organic chemistry. It serves as a key intermediate in the production of pharmaceuticals, particularly in the development of drugs that require specific stereochemistry for enhanced efficacy. Commonly employed in research laboratories for studying enzyme-substrate interactions and in the preparation of modified amino acids for biochemical studies. Its stability and solubility make it suitable for various chemical reactions, including esterification and amidation processes.

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