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Catalog Number:
24757
CAS Number:
105382-08-9
HD-HoPhe-OH·HCl
Purity:
≥ 99%
Synonym(s):
Clorhidrato de ácido (R)-2-amino-4-fenilbutírico
Documents
$37.96 /1G
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Product Information

H-D-HoPhe-OH·HCl, also known as (2R)-2-amino-4-phenylbutanoic acid hydrochloride, is a versatile compound widely utilized in pharmaceutical research and development. This hydrochloride salt form enhances its solubility, making it particularly useful in various biological assays and formulations. Researchers often employ H-D-HoPhe-OH·HCl in peptide synthesis and as a building block in the development of novel therapeutic agents, especially in the field of neuropharmacology. Its unique structure allows for specific interactions with biological targets, which can lead to the discovery of new drugs with improved efficacy and safety profiles.

In addition to its applications in drug development, H-D-HoPhe-OH·HCl serves as a valuable tool in studying amino acid metabolism and protein interactions. Its ability to mimic natural amino acids makes it an ideal candidate for exploring metabolic pathways and enzyme activities. With its favorable properties and diverse applications, H-D-HoPhe-OH·HCl stands out as an essential compound for researchers aiming to innovate in the pharmaceutical and biochemical fields.

Synonyms
Clorhidrato de ácido (R)-2-amino-4-fenilbutírico
CAS Number
105382-08-9
Purity
≥ 99%
Molecular Formula
C10H13NO2 · HCl
Molecular Weight
215.72
MDL Number
MFCD09832068
PubChem ID
20137834
Melting Point
230 °C (descenso)
Appearance
Polvo blanco
Optical Rotation
[a] 25 D = -36 ± 1 ° (C=1 en HCl 3N)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Clorhidrato de ácido (R)-2-amino-4-fenilbutírico
CAS Number
105382-08-9
Purity
≥ 99%
Molecular Formula
C10H13NO2 · HCl
Molecular Weight
215.72
MDL Number
MFCD09832068
PubChem ID
20137834
Melting Point
230 °C (descenso)
Appearance
Polvo blanco
Optical Rotation
[a] 25 D = -36 ± 1 ° (C=1 en HCl 3N)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

H-D-HoPhe-OH·HCl is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, which are crucial for developing new drugs and therapies in the pharmaceutical industry.
  • Neuroscience Research: It is used in studies related to neurotransmitter function and neuropharmacology, helping researchers understand brain functions and develop treatments for neurological disorders.
  • Biochemical Assays: The compound is employed in various biochemical assays to study enzyme activity and protein interactions, providing insights into cellular processes.
  • Drug Development: Its unique properties make it valuable in the formulation of novel therapeutic agents, particularly in targeting specific biological pathways.
  • Cosmetic Applications: H-D-HoPhe-OH·HCl is explored in cosmetic formulations for its potential benefits in skin care, promoting skin health and appearance.

Citas