1668-10-6

2-Aminoacetamide hydrochloride Chemical Structure
1668-10-6

Chemical Structure

2-Aminoacetamide hydrochloride

Synonym(s): Glycinamide hydrochloride

  • CAS No.: 1668-10-6
  • Formula:C2H7ClN2O
  • Molecular Weight:110.54

IUPAC Name: 2-aminoacetamide hydrochloride

InChIKey: WKNMKGVLOWGGOU-UHFFFAOYSA-N

SMILES: O=C(N)CN.Cl

Biological Activity: 2-Aminoacetamide hydrochloride (Glycinamide hydrochloride) is a derivative of Glycine (HY-Y0966). 2-Aminoacetamide hydrochloride forms cell-absorbable nanocomplexes with proteins (such as bovine serum albumin) through strong electrostatic interactions, promoting cellular uptake of related proteins. 2-Aminoacetamide hydrochloride synergizes with BMP2 to upregulate the expression of osteogenic marker genes (such as Col1a1, Alp, Runx2) and proteins (such as COL1, BSP), enhancing collagen synthesis. 2-Aminoacetamide hydrochloride synergizes with BMP2 to promote osteoblast differentiation in vitro and bone regeneration in vivo[1].

Cat. No. Product Name Purity Description Pricing
HY-Y1123
2-Aminoacetamide hydrochloride 99.83% 2-Aminoacetamide hydrochloride (Glycinamide hydrochloride) is a derivative of Glycine (HY-Y0966). 2-Aminoacetamide hydrochloride forms cell-absorbable nanocomplexes with proteins (such as bovine serum albumin) through strong electrostatic interactions, promoting cellular uptake of related proteins. 2-Aminoacetamide hydrochloride synergizes with BMP2 to upregulate the expression of osteogenic marker genes (such as Col1a1, Alp, Runx2) and proteins (such as COL1, BSP), enhancing collagen synthesis. 2-Aminoacetamide hydrochloride synergizes with BMP2 to promote osteoblast differentiation in vitro and bone regeneration in vivo.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References