Cas no 7662-51-3 (L-Tyrosine Hydrazide)

L-Tyrosine Hydrazide is a derivative of the amino acid L-tyrosine, modified with a hydrazide functional group. This compound is primarily utilized in peptide synthesis and biochemical research, where it serves as a versatile building block for the introduction of tyrosine residues with enhanced reactivity. The hydrazide moiety enables selective conjugation and modification, making it valuable for applications such as crosslinking, labeling, and the preparation of hydrazone-based probes. Its stability and compatibility with standard peptide coupling reagents further enhance its utility in solid-phase and solution-phase synthesis. Researchers favor L-Tyrosine Hydrazide for its precise functionalization potential and reliability in complex chemical workflows.
L-Tyrosine Hydrazide structure
L-Tyrosine Hydrazide structure
Product Name:L-Tyrosine Hydrazide
CAS No:7662-51-3
MF:C9H13N3O2
MW:195.218421697617
MDL:MFCD00007609
CID:566140
PubChem ID:87577551
Update Time:2025-06-08

L-Tyrosine Hydrazide Chemical and Physical Properties

Names and Identifiers

    • (S)-2-Amino-3-(4-hydroxyphenyl)propanehydrazide
    • L-Tyrosine Hydrazide
    • <small>L<
    • H-TYR-NHNH2
    • l-thyrosine hydrazide
    • L-Tyrosin-hydrazid
    • L-tyrosinohydrazide
    • Tyrosinehydrazide
    • Tyrosine, hydrazide, L-
    • L-Tyrosine, hydrazide
    • MWIXENPCUPDSOS-QMMMGPOBSA-N
    • (2S)-2-amino-3-(4-hydroxyphenyl)propanehydrazide
    • L-Tyrosinehydrazide
    • tyrosine hydrazone
    • tyrosine hydrazide
    • KM1782
    • BDBM50200191
    • 1933AC
    • HY-W142000
    • NSC 337746
    • CHEMBL220460
    • AS-67360
    • CS-0201786
    • SCHEMBL4668353
    • MFCD00007609
    • D92529
    • DTXSID90884412
    • AKOS016843145
    • L-Tyrosine hydrazide, 98%
    • T1820
    • AC-24157
    • 2-Amino-3-(4-hydroxyphenyl)propanohydrazide #
    • EINECS 231-631-1
    • 7662-51-3
    • T-9300
    • MDL: MFCD00007609
    • Inchi: 1S/C9H13N3O2/c10-8(9(14)12-11)5-6-1-3-7(13)4-2-6/h1-4,8,13H,5,10-11H2,(H,12,14)/t8-/m0/s1
    • InChI Key: MWIXENPCUPDSOS-QMMMGPOBSA-N
    • SMILES: O=C([C@H](CC1C=CC(=CC=1)O)N)NN

Computed Properties

  • Exact Mass: 195.10100
  • Monoisotopic Mass: 195.100776666g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 3
  • Complexity: 191
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -1
  • Topological Polar Surface Area: 101

Experimental Properties

  • Color/Form: Not determined
  • Density: 1.1985 (rough estimate)
  • Melting Point: 196-198?°C (lit.)
  • Boiling Point: 331.89°C (rough estimate)
  • Flash Point: 250.6±27.3 °C
  • Refractive Index: 78 ° (C=5, 1mol/L HCl)
  • PSA: 101.37000
  • LogP: 1.04340
  • Optical Activity: [α]20/D +76°, c =?4.2 in 1 M HCl
  • Vapor Pressure: 0.0±1.3 mmHg at 25°C

L-Tyrosine Hydrazide Security Information

L-Tyrosine Hydrazide Customs Data

  • HS CODE:2928000090
  • Customs Data:

    China Customs Code:

    2928000090

    Overview:

    2928000090 Other hydrazine(Hydrazine)And chlorhexidine(hydroxylamine)Organic derivatives of.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

L-Tyrosine Hydrazide Pricemore >>

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TRC
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Additional information on L-Tyrosine Hydrazide

L-Tyrosine Hydrazide (CAS No. 7662-51-3): An Overview of Its Structure, Applications, and Recent Research

L-Tyrosine Hydrazide (CAS No. 7662-51-3) is a versatile compound with significant applications in various fields, including pharmaceuticals, biochemistry, and materials science. This compound is derived from the amino acid L-tyrosine and is characterized by its unique chemical structure and reactivity. In this comprehensive overview, we will delve into the structural properties, applications, and recent research advancements of L-Tyrosine Hydrazide.

Chemical Structure and Properties

L-Tyrosine Hydrazide is a white crystalline solid with the molecular formula C9H13N3O2. It has a molecular weight of 195.21 g/mol. The compound is synthesized by reacting L-tyrosine with hydrazine, resulting in the formation of a hydrazide functional group (-NH-NH2) at the carboxyl end of the amino acid. This unique structure imparts L-Tyrosine Hydrazide with several important properties:

  • Solubility: It is soluble in water and polar organic solvents such as methanol and ethanol.
  • Reactivity: The hydrazide group makes it highly reactive towards carbonyl compounds, allowing it to form stable hydrazone derivatives.
  • Stability: It is stable under normal laboratory conditions but may degrade upon exposure to strong acids or bases.

Applications in Pharmaceuticals and Biochemistry

L-Tyrosine Hydrazide has found extensive use in pharmaceutical research and development due to its ability to form stable complexes with metal ions and its potential as a building block for drug molecules. Some key applications include:

  • Metal Chelation: The compound can form stable complexes with transition metals, which is useful in the development of metal-based drugs and imaging agents.
  • Bioconjugation: It can be used to conjugate biomolecules such as proteins and peptides, enhancing their stability and bioavailability.
  • Drug Delivery Systems: The hydrazide group can be used to create prodrugs that are activated under specific physiological conditions, improving drug targeting and efficacy.

L-Tyrosine Hydrazide has also been explored for its potential in treating neurodegenerative diseases. Recent studies have shown that derivatives of L-tyrosine can modulate neurotransmitter levels and protect neurons from oxidative stress. For example, a study published in the Journal of Medicinal Chemistry demonstrated that a derivative of L-Tyrosine Hydrazide exhibited neuroprotective effects in an animal model of Parkinson's disease.

Molecular Biology and Materials Science Applications strong>

Beyond pharmaceuticals, L-Tyrosine Hydrazide strong> has found applications in molecular biology and materials science. In molecular biology, it is used as a reagent for labeling proteins and nucleic acids. The hydrazide group can react with aldehyde or ketone groups on biomolecules, allowing for site-specific labeling and detection.

In materials science, < strong>L-Tyrosine Hydrazide< / strong > has been utilized in the synthesis of advanced polymers and nanomaterials. Its reactivity with carbonyl compounds makes it an excellent cross-linking agent for creating robust polymer networks. For instance, researchers at the University of California have developed biodegradable hydrogels using L-tyrosine-based monomers, which have potential applications in tissue engineering and drug delivery systems. p > < p >< strong >Recent Research Advancements< / strong > p > < p >The field of research surrounding< strong >L-Tyrosine Hydrazide< / strong > continues to expand, driven by its diverse chemical properties and potential applications. One notable area of recent research is its use in developing novel antimicrobial agents. A study published in the Journal of Antibiotics reported that a series of L-tyrosine-derived hydrazides exhibited potent antibacterial activity against both Gram-positive and Gram-negative bacteria. This finding opens up new possibilities for combating antibiotic-resistant pathogens. p > < p >Another area of interest is the use of< strong >L-Tyrosine Hydrazide< / strong > in green chemistry. Researchers at the University of Cambridge have developed an environmentally friendly method for synthesizing this compound using renewable feedstocks. This approach not only reduces the environmental impact but also enhances the sustainability of chemical production processes. p > < p >< strong >Conclusion< / strong > p > < p >< strong >L-Tyrosine Hydrazide (CAS No. 7662-51-3)< / strong > is a multifaceted compound with a wide range of applications in pharmaceuticals, biochemistry, molecular biology, and materials science. Its unique chemical structure and reactivity make it an invaluable tool for researchers across various disciplines. As ongoing research continues to uncover new properties and applications, the importance of this compound is likely to grow even further. p > article > response >

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