L-allo-Threonine

99%

Reagent Code: #105254
label
Alias L-Allothreonine; (2S,3S)-2-amino-3-hydroxybutyric acid
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CAS Number 28954-12-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 119.12 g/mol
Formula C₄H₉NO₃
badge Registry Numbers
EC Number 249-327-2
MDL Number MFCD00064268
thermostat Physical Properties
Melting Point 272 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

L-allo-Threonine is primarily used in biochemical research and pharmaceutical development. It serves as a key component in the study of amino acid metabolism and protein synthesis. In the pharmaceutical industry, it is utilized in the production of specialized drugs and therapeutic agents, particularly those targeting metabolic disorders or requiring specific amino acid configurations. Additionally, it plays a role in the development of nutritional supplements designed to support muscle growth and repair. Its unique stereochemistry makes it valuable in the synthesis of peptides and other bioactive compounds.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 99-100%
Specific Rotation [α]20/D (C=2, Water) 8-10
Appearance White To Off-White Powder Or Crystals
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿550.00
inventory 1g
10-20 days ฿990.00
inventory 5g
10-20 days ฿2,750.00
inventory 25g
10-20 days ฿12,750.00
L-allo-Threonine
L-allo-Threonine is primarily used in biochemical research and pharmaceutical development. It serves as a key component in the study of amino acid metabolism and protein synthesis. In the pharmaceutical industry, it is utilized in the production of specialized drugs and therapeutic agents, particularly those targeting metabolic disorders or requiring specific amino acid configurations. Additionally, it plays a role in the development of nutritional supplements designed to support muscle growth and repair. Its unique stereochemistry makes it valuable in the synthesis of peptides and other bioactive compounds.
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