Serinol hydrochloride

98%

Reagent Code: #134542
label
Alias Serine alcohol hydrochloride;2-amino-1,3-propanediol hydrochloride
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CAS Number 73708-65-3

science Other reagents with same CAS 73708-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 127.57 g/mol
Formula HOCH₂CH(NH₂)CH₂OH·HCl
badge Registry Numbers
MDL Number MFCD00012592
thermostat Physical Properties
Melting Point 106-108 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a building block in organic synthesis, particularly in the preparation of nucleosides and nucleotides. It serves as a chiral scaffold in pharmaceuticals and bioactive compounds due to its stereochemistry and functional groups. Commonly employed in the synthesis of antiviral and anticancer agents. Also utilized in the development of modified sugars and glycoconjugates for biochemical research. Its hydrochloride salt form enhances solubility and stability in aqueous environments, making it suitable for solution-phase reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,500.00
inventory 250mg
10-20 days ฿4,760.00
inventory 1g
10-20 days ฿7,700.00

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Serinol hydrochloride
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Used as a building block in organic synthesis, particularly in the preparation of nucleosides and nucleotides. It serves as a chiral scaffold in pharmaceuticals and bioactive compounds due to its stereochemistry and functional groups. Commonly employed in the synthesis of antiviral and anticancer agents. Also utilized in the development of modified sugars and glycoconjugates for biochemical research. Its hydrochloride salt form enhances solubility and stability in aqueous environments, making it suitable

Used as a building block in organic synthesis, particularly in the preparation of nucleosides and nucleotides. It serves as a chiral scaffold in pharmaceuticals and bioactive compounds due to its stereochemistry and functional groups. Commonly employed in the synthesis of antiviral and anticancer agents. Also utilized in the development of modified sugars and glycoconjugates for biochemical research. Its hydrochloride salt form enhances solubility and stability in aqueous environments, making it suitable for solution-phase reactions.

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