2-[[(2S)-2-[(2-aminoacetyl)amino]propanoyl]amino]acetic Acid

Base Information

• Chemical Name: 2-[[(2S)-2-[(2-aminoacetyl)amino]propanoyl]amino]acetic Acid
• CAS No.: 16422-05-2
• Molecular Formula: C₇H₁₃N₃O₄
• Molecular Weight: 203.198
• Hs Code.: 2924199090
• DSSTox Substance ID: DTXSID30427403
• Nikkaji Number: J653.924F
• Metabolomics Workbench ID: 81863
• Mol file: 16422-05-2.mol

Synonyms:H-Gly-Ala-Gly-OH;16422-05-2;glycylalanylglycine;Gly-Ala-Gly;2-[[(2S)-2-[(2-aminoacetyl)amino]propanoyl]amino]acetic Acid;Glycyl-L-alanylglycine;(S)-2-(2-(2-Aminoacetamido)propanamido)acetic acid;Gly-Ala-Gly-OH;Glycyl-alanyl-glycine;Glycyl-L-alanyl-glycine;SCHEMBL11656504;DTXSID30427403;CHEBI:163420;UGVQELHRNUDMAA-BYPYZUCNSA-N;HY-P4230;MFCD00083689;AKOS022181526;CS-0653232;2-[(2S)-2-(2-aminoacetamido)propanamido]acetic acid;2-[[(2S)-2-[(2-azaniumylacetyl)amino]propanoyl]amino]acetate

Chemical Property of 2-[[(2S)-2-[(2-aminoacetyl)amino]propanoyl]amino]acetic Acid

Chemical Property:

• Vapor Pressure: 3.53E-16mmHg at 25°C
• Refractive Index: 1.517
• Boiling Point: 604.6°C at 760 mmHg
• Flash Point: 319.5°C
• PSA: 121.52000
• Density: 1.314g/cm³
• LogP: -0.86730
• Storage Temp.: -15°C
• XLogP3: -4.3
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 203.09060590
• Heavy Atom Count: 14
• Complexity: 241

Purity/Quality:

99% ^*data from raw suppliers

H-Gly-Ala-Gly-OH ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C(=O)NCC(=O)O)NC(=O)CN
• Isomeric SMILES: C[C@@H](C(=O)NCC(=O)O)NC(=O)CN

Technology Process of 2-[[(2S)-2-[(2-aminoacetyl)amino]propanoyl]amino]acetic Acid

There total 5 articles about 2-[[(2S)-2-[(2-aminoacetyl)amino]propanoyl]amino]acetic Acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

N-carbobenzoxyglycyl-L-alanylglycine benzyl ester (7801-73-2) → Gly-Ala-Gly (16422-05-2,53298-65-0)

Guidance literature:

With hydrogen; palladium on activated charcoal; In water; acetone;

DOI:10.1007/BF00650418

Reference yield:

→ Gly-Ala-Gly (16422-05-2,53298-65-0)

Guidance literature:

With palladium; acetic acid; Hydrogenation;

DOI:10.1021/ja01151a513

Reference yield:

(S)-2-(2-Benzyloxycarbonylamino-acetylamino)-propionic acid (3079-63-8) → Gly-Ala-Gly (16422-05-2,53298-65-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 62 percent / N,N'-dicyclohexylcarbodiimide

2: 90 percent / H₂ / Pd/C / acetone; H₂O

With hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal; In water; acetone;

DOI:10.1007/BF00650418

upstream raw materials:

N-carbobenzoxyglycyl-L-alanylglycine benzyl ester

(S)-2-(2-Benzyloxycarbonylamino-acetylamino)-propionic acid

Refernces

Thermodynamic properties of peptide solutions 3. Partial molar volumes and partial molar heat capacities of some tripeptides in aqueous solution

10.1007/BF00650418

The research investigates the thermodynamic properties of certain tripeptides in aqueous solution. The study aims to understand the effects of side chain position on solute-solvent interactions in peptides, which can provide insights into the conformational stability and unfolding behavior of proteins. The key chemicals used in the research are four tripeptides: glycylglycylglycine (GGG), glycylglycylalanine (GGA), glycylalanylglycine (GAG), and alanylglycylglycine (AGG). The researchers measured the partial molar volumes and partial molar heat capacities of these tripeptides at 25°C. The results showed that the tripeptide-water interaction is influenced by the side chain position within the molecule. For instance, the partial molar volume and heat capacity varied depending on whether the methyl side chain was adjacent to the -NH2 or -COO- end group. The study concluded that a tripeptide with a side chain in the central position is a reasonable model for investigating side chain effects in polypeptides, and the data obtained can help in understanding the contribution of various non-covalent interactions in protein folding and stability.

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