D-2,3-Diaminopropionic acid monohydrochloride

99%

Reagent Code: #104896
label
Alias (R)-(-)-2,3-Diaminopropionic acid hydrochloride
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CAS Number 6018-56-0

science Other reagents with same CAS 6018-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 140.57 g/mol
Formula C₃H₈N₂O₂HCl
badge Registry Numbers
MDL Number MFCD00070606
thermostat Physical Properties
Melting Point 232 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used in biochemical research as a building block for peptide synthesis, particularly in the study of enzyme mechanisms and protein interactions. It serves as a precursor for the synthesis of specialized amino acids and compounds with potential therapeutic applications. In medicinal chemistry, it is employed to develop analogs of natural amino acids for drug discovery, targeting neurological and metabolic disorders. Additionally, it is utilized in the production of chiral catalysts and ligands for asymmetric synthesis in organic chemistry. Its role in studying neurotransmission and receptor binding is also significant in neuroscience research.

format_list_bulleted Product Specification

Test Parameter Specification
Melting Point 235-240
Purity (Neutralization Titration) 98.5-101.5
Specific Rotation [α]20/D (C=2, 1 Mol/L HCl) -26 to -20
HCl -26 to -20
Appearance White to light yellow powder or crystals
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿530.00
inventory 1g
10-20 days ฿920.00
inventory 5g
10-20 days ฿3,420.00
inventory 25g
10-20 days ฿15,310.00

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D-2,3-Diaminopropionic acid monohydrochloride
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Used in biochemical research as a building block for peptide synthesis, particularly in the study of enzyme mechanisms and protein interactions. It serves as a precursor for the synthesis of specialized amino acids and compounds with potential therapeutic applications. In medicinal chemistry, it is employed to develop analogs of natural amino acids for drug discovery, targeting neurological and metabolic disorders. Additionally, it is utilized in the production of chiral catalysts and ligands for asymmet

Used in biochemical research as a building block for peptide synthesis, particularly in the study of enzyme mechanisms and protein interactions. It serves as a precursor for the synthesis of specialized amino acids and compounds with potential therapeutic applications. In medicinal chemistry, it is employed to develop analogs of natural amino acids for drug discovery, targeting neurological and metabolic disorders. Additionally, it is utilized in the production of chiral catalysts and ligands for asymmetric synthesis in organic chemistry. Its role in studying neurotransmission and receptor binding is also significant in neuroscience research.

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