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Catalog Number:
07991
CAS Number:
6319-96-6
ClAc-Gly-OH
Purity:
≥ 99% (TLC)
Synonym(s):
Chloracetyl glycine, (2-Chloro-acetylamino)-acetic acid
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Product Information

ClAc-Gly-OH, also known as 2-[(2-chloroacetyl)amino]acetic acid, is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This compound features a chloroacetyl group that enhances its reactivity, making it an excellent choice for peptide synthesis and modification. Researchers often employ ClAc-Gly-OH as a building block in the development of peptide-based drugs, where its unique functional groups facilitate the introduction of various amino acids, thereby tailoring the properties of the resulting peptides for specific therapeutic targets.

In addition to its role in peptide synthesis, ClAc-Gly-OH has shown potential in the field of drug delivery systems, where it can be used to create conjugates that improve the solubility and bioavailability of poorly soluble drugs. Its ability to form stable linkages with other biomolecules makes it a valuable tool for developing targeted therapies. With its diverse applications and ability to enhance drug efficacy, ClAc-Gly-OH stands out as a crucial compound for researchers and industry professionals focused on innovative therapeutic solutions.

Synonyms
Chloracetyl glycine, (2-Chloro-acetylamino)-acetic acid
CAS Number
6319-96-6
Purity
≥ 99% (TLC)
Molecular Formula
C4H6ClNO3
Molecular Weight
151.55
MDL Number
MFCD00021733
PubChem ID
233485
Melting Point
105 - 109 ºC
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Chloracetyl glycine, (2-Chloro-acetylamino)-acetic acid
CAS Number
6319-96-6
Purity
≥ 99% (TLC)
Molecular Formula
C4H6ClNO3
Molecular Weight
151.55
MDL Number
MFCD00021733
PubChem ID
233485
Melting Point
105 - 109 ºC
Appearance
White powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

ClAc-Gly-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, which are essential for developing new drugs and therapies.
  • Bioconjugation: It is used in bioconjugation processes to link biomolecules, enhancing the efficacy of targeted drug delivery systems in cancer treatment.
  • Research in Neurobiology: ClAc-Gly-OH is applied in studies related to neurotransmitter functions, aiding in the understanding of neurological disorders.
  • Diagnostic Reagents: This chemical acts as a reagent in various diagnostic tests, improving the accuracy of biochemical assays.
  • Antibody Labeling: It is utilized for labeling antibodies in immunoassays, facilitating better detection and quantification of proteins in research.

Citations