L-2,4-Diaminobutyric acid hydrochloride
98%
Reagent
Code: #105210
Alias
L-2,4-diaminobutyric acid dihydrochloride
CAS Number
1883-09-6
blur_circular Chemical Specifications
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Molecular Information
Weight
191.06 g/mol
Formula
C₄H₁₀N₂O₂₂HCl
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Registry Numbers
EC Number
217-542-0
MDL Number
MFCD00064561
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Physical Properties
Melting Point
197-200 °C (dec.)
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Storage & Handling
Storage
Room temperature, dry, sealed
description Product Description
L-2,4-Diaminobutyric acid hydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of various biologically active compounds, including peptides and amino acid derivatives. Its role in studying metabolic pathways, particularly those involving amino acid metabolism, is significant. Additionally, it is utilized in the development of drugs targeting specific enzymes or receptors due to its structural similarity to naturally occurring amino acids. In some cases, it is also employed in the preparation of chiral catalysts for asymmetric synthesis, enhancing the efficiency and selectivity of chemical reactions.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (HPLC) | 98-100 |
Purity (Titration with AgNO3) | 97.5-102.5 |
Specific Rotation [α]20/D (C=3.6, H2O) | 13-16 |
Sulfated Ash | 0-0.1 |
Water (Karl Fischer) | 0-2.5 |
Appearance | White To Off-White To Light Yellow Powder Or Crystals |
Infrared Spectrum | Conforms To Structure |
Solubility in Water | Very Faint Turbidity |
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L-2,4-Diaminobutyric acid hydrochloride
L-2,4-Diaminobutyric acid hydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of various biologically active compounds, including peptides and amino acid derivatives. Its role in studying metabolic pathways, particularly those involving amino acid metabolism, is significant. Additionally, it is utilized in the development of drugs targeting specific enzymes or receptors due to its structural similarity to naturally occurring amino acids. In some cases, it is also employed in the preparation of chiral catalysts for asymmetric synthesis, enhancing the efficiency and selectivity of chemical reactions.
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