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Catalog Number:
12796
CAS Number:
19914-38-6
Boc-N-methyl-D-alanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-N-Me-D-Ala-OH, (R-2-(tert-Butoxycarbonyl-methyl-amino)propionic acid
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Product Information

Boc-N-methyl-D-alanine is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and facilitates the selective modification of amino acids in various synthetic pathways. Its unique structure allows for the incorporation of methyl groups, making it an essential building block for the development of bioactive peptides and drug candidates. Researchers appreciate its role in enhancing the solubility and bioavailability of peptides, which is crucial for therapeutic applications.

In addition to its significance in peptide synthesis, Boc-N-methyl-D-alanine is also employed in the study of protein interactions and enzyme mechanisms. Its ability to mimic natural amino acids while providing distinct chemical properties makes it an excellent tool for exploring structure-activity relationships in drug design. This compound is particularly advantageous for those looking to develop novel therapeutics with improved efficacy and reduced side effects. With its diverse applications in medicinal chemistry and biochemistry, Boc-N-methyl-D-alanine stands out as a versatile and essential reagent for researchers and industry professionals alike.

Synonyms
Boc-N-Me-D-Ala-OH, (R-2-(tert-Butoxycarbonyl-methyl-amino)propionic acid
CAS Number
19914-38-6
Purity
≥ 98% (HPLC)
Molecular Formula
C9H17NO4
Molecular Weight
203.2
MDL Number
MFCD00063137
PubChem ID
4436857
Melting Point
78-87 ?C
Optical Rotation
[a]D25 = + 32 ± 2 º (C=1.127 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-N-Me-D-Ala-OH, (R-2-(tert-Butoxycarbonyl-methyl-amino)propionic acid
CAS Number
19914-38-6
Purity
≥ 98% (HPLC)
Molecular Formula
C9H17NO4
Molecular Weight
203.2
MDL Number
MFCD00063137
PubChem ID
4436857
Melting Point
78-87 ?C
Optical Rotation
[a]D25 = + 32 ± 2 º (C=1.127 in MeOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-N-methyl-D-alanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of pharmaceuticals. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In medicinal chemistry, Boc-N-methyl-D-alanine is used to create analogs of biologically active compounds. Its structural properties can lead to improved potency and selectivity in drug candidates.
  • Biotechnology: This chemical is employed in the production of modified proteins and enzymes, which can be used in various biotechnological applications, including diagnostics and therapeutics.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter systems, where its structural similarities to amino acids can help in understanding receptor interactions and signaling pathways.
  • Custom Synthesis: Many research labs leverage Boc-N-methyl-D-alanine for custom synthesis projects, allowing for tailored compounds that meet specific research needs, which can lead to innovative discoveries.

Citations