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Catalog Number:
09042
CAS Number:
163750-76-3
H-D-His(3-Me)-OH
Purity:
≥ 99% (TLC)
Synonym(s):
D-His(π-Me)-OH, H-N-π-methyl-D-histidine
Documents
$120.88 /25MG
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Product Information

H-D-His(3-Me)-OH, also known as 3-Methyl-Histidine, is a valuable amino acid derivative that plays a crucial role in various biochemical applications. This compound is particularly significant in the fields of biochemistry and pharmaceuticals, where it is utilized as a building block for peptide synthesis and as a research tool in studying protein interactions and enzyme activities. Its unique structure, featuring a 3-methyl group on the imidazole ring, enhances its stability and solubility, making it an ideal candidate for formulating biologically active compounds.

Researchers and industry professionals can leverage H-D-His(3-Me)-OH in the development of novel therapeutics, particularly in the study of metabolic pathways and muscle physiology. Its application extends to the synthesis of peptide-based drugs, where it can improve the pharmacological properties of therapeutic agents. Additionally, its role in muscle metabolism makes it a subject of interest in sports science and nutrition research. By incorporating H-D-His(3-Me)-OH into their studies, professionals can gain deeper insights into protein dynamics and metabolic regulation, ultimately leading to advancements in health and medicine.

Synonyms
D-His(π-Me)-OH, H-N-π-methyl-D-histidine
CAS Number
163750-76-3
Purity
≥ 99% (TLC)
Molecular Formula
C7H11N3O2
Molecular Weight
169.18
MDL Number
MFCD00067633
PubChem ID
565965
Appearance
Slightly yellowish powder
Optical Rotation
[a]D24 = +23 ± 2º (C=1% in Water)
Conditions
Store at 0-8°C
General Information
Synonyms
D-His(π-Me)-OH, H-N-π-methyl-D-histidine
CAS Number
163750-76-3
Purity
≥ 99% (TLC)
Molecular Formula
C7H11N3O2
Molecular Weight
169.18
MDL Number
MFCD00067633
PubChem ID
565965
Appearance
Slightly yellowish powder
Optical Rotation
[a]D24 = +23 ± 2º (C=1% in Water)
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

H-D-His(3-Me)-OH is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require histidine derivatives, enhancing the stability and functionality of the resulting peptides.
  • Biochemical Research: Researchers use it to study enzyme activity and protein interactions, as its unique structure allows for the exploration of histidine's role in various biochemical pathways.
  • Drug Development: The compound is valuable in pharmaceutical research for developing new drugs, especially those targeting histamine receptors, due to its structural similarity to natural histidine.
  • Diagnostics: It can be utilized in diagnostic assays to detect specific biomolecules, aiding in the early diagnosis of diseases by improving the sensitivity of detection methods.
  • Food Industry: H-D-His(3-Me)-OH is explored for its potential in enhancing flavor profiles in food products, leveraging its amino acid characteristics to improve taste and nutritional value.

Citations