L-Alaninamide hydrochloride
Chemical Name
(2S)-2-aminopropanamide;hydrochloride
L-Alaninamide hydrochloride•Nitrogen Compound (Non-heterocyclic)
Structure: 
Product No
CH59005
CAS
33208-99-0
MF
C3H9ClN2O
MW
124.57
Specification
| Catalog No. | CH59005 |
| CAS No. | 33208-99-0 |
| Molecular Formula | C3H9ClN2O |
| Molecular Weight | 124.57 |
CHEMOS Support for This Category
CHEMOS supports non-heterocyclic nitrogen building blocks, including amines, amino alcohols, nitriles, carbamates, and protected intermediates. Chiral amine chemistry : chiral-pool synthesis, resolution, and stereochemical-control strategies. Protecting-group chemistry : Boc, Cbz, Fmoc, and tailored protection or deprotection sequences. Reactive intermediate handling : project-specific safety review for amines, nitriles, and related functional groups. Analytical support : identity, purity, water content, and residual-solvent testing can be discussed. Process development : route refinement and scale-up planning according to target specification.
Overview
L-Alaninamide hydrochloride (also known as (2S)-2-aminopropanamide;hydrochloride) (CAS 33208-99-0, MF C3H9ClN2O, MW 124.57) is a nitrogen-functionalised organic intermediate used in medicinal chemistry and ligand synthesis. Programs working with this compound usually examine route flexibility for downstream substitution, stereo-purity, and impurity control. Bench-scale to larger-scale production is supported through CHEMOS organic chemistry workflows and dedicated process-development resources.
Applications
- L-Alaninamide hydrochloride (33208-99-0) as a starting point for downstream chemistry programs
- Custom synthesis of N-protected variants on request
- Reference material in peptide and PROTAC-linker chemistry programs
- Amide-bond formation and reductive amination substrate
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