(S)-Piperidine-2-carboxylic acid hydrochloride

95%

Reagent Code: #121193
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CAS Number 2133-33-7

science Other reagents with same CAS 2133-33-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.62 g/mol
Formula C₆H₁₂ClNO₂
badge Registry Numbers
MDL Number MFCD00066139
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a chiral building block for the synthesis of various drugs, particularly those targeting neurological disorders. It serves as a precursor in the production of enantiomerically pure compounds, enhancing the efficacy and specificity of therapeutic agents. Additionally, it is employed in the development of peptide mimetics and bioactive molecules due to its structural similarity to natural amino acids. Its hydrochloride form improves solubility, making it suitable for use in aqueous-based formulations and laboratory experiments.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Specific Rotation [α]20/D (C=1, H2O) -12.5 to -10.5

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿4,670.00
inventory 1g
10-20 days ฿420.00
inventory 5g
10-20 days ฿1,200.00

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(S)-Piperidine-2-carboxylic acid hydrochloride
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Used in pharmaceutical research as a chiral building block for the synthesis of various drugs, particularly those targeting neurological disorders. It serves as a precursor in the production of enantiomerically pure compounds, enhancing the efficacy and specificity of therapeutic agents. Additionally, it is employed in the development of peptide mimetics and bioactive molecules due to its structural similarity to natural amino acids. Its hydrochloride form improves solubility, making it suitable for use

Used in pharmaceutical research as a chiral building block for the synthesis of various drugs, particularly those targeting neurological disorders. It serves as a precursor in the production of enantiomerically pure compounds, enhancing the efficacy and specificity of therapeutic agents. Additionally, it is employed in the development of peptide mimetics and bioactive molecules due to its structural similarity to natural amino acids. Its hydrochloride form improves solubility, making it suitable for use in aqueous-based formulations and laboratory experiments.

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