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Catalog Number:
00606
CAS Number:
34306-42-8
Boc-L-α-aminobutyric acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-Abu-OH, Boc-L-2-aminobutanoic acid
Documents
$18.53 /1G
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Product Information

Boc-L-a-aminobutyric acid is a valuable compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for various applications in organic synthesis. Researchers often employ Boc-L-a-aminobutyric acid in the development of bioactive peptides and as a building block in the synthesis of complex molecules. Its unique structure allows for selective reactions, facilitating the creation of diverse compounds with potential therapeutic properties.

In addition to its role in peptide synthesis, Boc-L-a-aminobutyric acid has shown promise in the field of drug development, particularly in the design of inhibitors and modulators for various biological targets. Its compatibility with standard coupling reagents and methodologies makes it a preferred choice for chemists looking to streamline their synthesis processes. With its robust performance and versatility, Boc-L-a-aminobutyric acid stands out as an essential tool for researchers and industry professionals aiming to innovate in the fields of medicinal chemistry and biochemistry.

Synonyms
Boc-L-Abu-OH, Boc-L-2-aminobutanoic acid
CAS Number
34306-42-8
Purity
≥ 98% (HPLC)
Molecular Formula
C9H17NO4
Molecular Weight
203.3
MDL Number
MFCD00037267
PubChem ID
333522
Appearance
White to off-white powder
Optical Rotation
+5.3° (c=1.5% MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Abu-OH, Boc-L-2-aminobutanoic acid
CAS Number
34306-42-8
Purity
≥ 98% (HPLC)
Molecular Formula
C9H17NO4
Molecular Weight
203.3
MDL Number
MFCD00037267
PubChem ID
333522
Appearance
White to off-white powder
Optical Rotation
+5.3° (c=1.5% 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-L-a-aminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without interference from other functional groups.
  • Drug Development: It plays a crucial role in the development of pharmaceutical compounds, particularly in creating prodrugs that enhance bioavailability and reduce side effects.
  • Biochemical Research: Researchers use it to study protein interactions and enzyme activities, providing insights into metabolic pathways and cellular functions.
  • Analytical Chemistry: The compound is employed in various analytical techniques, including chromatography, to separate and identify amino acids and related compounds effectively.
  • Cosmetic Formulations: Its properties are leveraged in the cosmetic industry for formulating skin care products, enhancing the stability and efficacy of active ingredients.

Citations