(S)-2-Amino-N-methylpropanamide hydrochloride

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Reagent Code: #52942
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CAS Number 61275-22-7

science Other reagents with same CAS 61275-22-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.60 g/mol
Formula C₄H₁₁ClN₂O
badge Registry Numbers
MDL Number MFCD00237739
thermostat Physical Properties
Boiling Point 257°C at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

Primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the production of chiral compounds, particularly in the development of drugs targeting neurological disorders and cardiovascular diseases. Its stereospecific properties make it valuable for creating enantiomerically pure substances, enhancing the efficacy and reducing side effects of medications. Additionally, it is employed in research laboratories for studying peptide synthesis and modifying amino acid derivatives to improve drug delivery systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,837.00
inventory 250mg
10-20 days ฿3,942.00
inventory 5g
10-20 days ฿33,624.00
inventory 10g
10-20 days ฿60,588.00

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(S)-2-Amino-N-methylpropanamide hydrochloride
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Primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the production of chiral compounds, particularly in the development of drugs targeting neurological disorders and cardiovascular diseases. Its stereospecific properties make it valuable for creating enantiomerically pure substances, enhancing the efficacy and reducing side effects of medications. Additionally, it is employed in research labo

Primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the production of chiral compounds, particularly in the development of drugs targeting neurological disorders and cardiovascular diseases. Its stereospecific properties make it valuable for creating enantiomerically pure substances, enhancing the efficacy and reducing side effects of medications. Additionally, it is employed in research laboratories for studying peptide synthesis and modifying amino acid derivatives to improve drug delivery systems.

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