methyl (2S)-2-((2S)-2-aminopropanamido)propanoate hydrochloride

Name: methyl (2S)-2-((2S)-2-aminopropanamido)propanoate hydrochloride
Brand: Creative Peptides
SKU: R2378
Availability: MadeToOrder

Methyl (2S)-2-((2S)-2-aminopropanamido)propanoate hydrochloride is a dipeptidyl methyl ester derived from alanine, useful as a chiral building block. The protonated amino group enhances solubility, while the ester allows controlled hydrolysis or coupling. Researchers study its conformational preferences and reactivity in peptide synthesis. Applications include fragment assembly, stereochemical probes, and linker design.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

methyl (2S)-2-((2S)-2-aminopropanamido)propanoate hydrochloride(CAS 41036-19-5)

CAT No: R2378

CAS No:41036-19-5

Synonyms/Alias:41036-19-5;H-ALA-ALA-OME HCL;(S)-Methyl 2-((S)-2-aminopropanamido)propanoate hydrochloride;H-Ala-Ala-OMe.HCl;H-Ala-Ala-OMe hydrochloride;methyl (2S)-2-[(2S)-2-aminopropanamido]propanoate hydrochloride;methyl (2S)-2-[[(2S)-2-aminopropanoyl]amino]propanoate;hydrochloride;methyl (2S)-2-((2S)-2-aminopropanamido)propanoate hydrochloride;MFCD00237711;H-Ala-Ala-OMe . HCl;SCHEMBL3883130;DTXSID00553440;BS-28147;E78489;EN300-100802;Methyl L-alanyl-L-alaninate--hydrogen chloride (1/1);831-614-4;

Custom Peptide Synthesis

cGMP Peptide

Registration of APIs
CMC information required for an IND

IND and NDA support
Drug master files (DMF) filing

M.F/Formula

C7H15ClN2O3

M.W/Mr.

210.66

Sequence

One Letter Code:AA
Three Letter Code:H-Ala-Ala-OMe.HCl

InChI

InChI=1S/C7H14N2O3.ClH/c1-4(8)6(10)9-5(2)7(11)12-3;/h4-5H,8H2,1-3H3,(H,9,10);1H/t4-,5-;/m0./s1

InChI Key

WVSVBOMWSCRPGM-FHAQVOQBSA-N

1. Immune-awakening Saccharomyces-inspired nanocarrier for oral target delivery to lymph and tumors

2. Extended exenatide administration enhances lipid metabolism and exacerbates pancreatic injury in mice on a high fat, high carbohydrate diet

3. Adipose tissue is a key organ for the beneficial effects of GLP-2 metabolic function

4. Implications of ligand-receptor binding kinetics on GLP-1R signalling

5. Application of human liver organoids as a patient-derived primary model for HBV infection and related hepatocellular carcinoma

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