Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
11928
CAS Number:
67183-18-0
Acide chloroacétyl-DL-2-amino- N -butyrique
Purity:
≥ 99 % (HPLC)
Synonym(s):
ClAc-DL-Abu-OH
Documents
$36.65 /1G
Taille
Request Bulk Quote
Product Information

Chloroacetyl-DL-2-amino-N-butyric acid is a versatile compound with significant applications in pharmaceutical and biochemical research. This amino acid derivative features a chloroacetyl group that enhances its reactivity, making it a valuable intermediate in the synthesis of various bioactive molecules. Researchers utilize this compound in the development of novel therapeutic agents, particularly in the fields of drug discovery and medicinal chemistry. Its unique structure allows for modifications that can lead to improved efficacy and specificity in targeting biological pathways.

In addition to its pharmaceutical applications, Chloroacetyl-DL-2-amino-N-butyric acid can also serve as a building block in peptide synthesis and the production of agrochemicals. Its ability to participate in diverse chemical reactions expands its utility in synthetic organic chemistry. By incorporating this compound into their research, scientists can explore innovative solutions to complex challenges in drug development and agricultural chemistry, ultimately contributing to advancements in health and environmental sustainability.

Synonyms
ClAc-DL-Abu-OH
CAS Number
67183-18-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H10NO3Cl
Molecular Weight
179.59
MDL Number
MFCD00055800
PubChem ID
307936
Melting Point
130-136 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
General Information
Synonyms
ClAc-DL-Abu-OH
CAS Number
67183-18-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H10NO3Cl
Molecular Weight
179.59
MDL Number
MFCD00055800
PubChem ID
307936
Melting Point
130-136 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Chloroacetyl-DL-2-amino-N-butyric acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs.
  • Biochemical Research: It is used in studies related to amino acid metabolism, helping researchers understand metabolic pathways and their implications in health and disease.
  • Peptide Synthesis: The compound plays a crucial role in the synthesis of peptides, which are essential for creating therapeutic agents and vaccines.
  • Analytical Chemistry: It is utilized as a standard in analytical methods to quantify amino acids and their derivatives, ensuring accuracy in research results.
  • Cosmetic Formulations: This chemical is incorporated into cosmetic products for its potential skin-conditioning properties, enhancing product efficacy and consumer appeal.

Citations