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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

L-Tyrosine, 3-amino-, dihydrochloride

OC(=O)[C@H](Cc1ccc(c(c1)N)O)N.Cl.Cl Request for Quotation
Chemical Name: L-Tyrosine, 3-amino-, dihydrochloride
CAS Number: 23279-22-3
Product Number: AG002MQO(AGN-PC-0QZN24)
Synonyms:
MDL No:
Molecular Formula: C9H14Cl2N2O3
Molecular Weight: 269.1251

Identification/Properties

Properties
MP:
158-160 °C (dec.)(lit.)
BP:
427.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
269.122g/mol
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
268.038g/mol
Monoisotopic Mass:
268.038g/mol
Topological Polar Surface Area:
110A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
210
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P302+P352-P304+P340-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-Tyr(3-NH2)-OH.2HCl, also known as Nα-(3-Aminotyrosine)-hydrochloride, is a valuable reagent in chemical synthesis due to its unique properties and applications. This compound is commonly used as a building block in peptide synthesis, specifically in the creation of peptides containing a tyrosine derivative. In chemical synthesis, H-Tyr(3-NH2)-OH.2HCl plays a crucial role in the modification of peptides and proteins to introduce specific functionalities or enhance their stability and bioactivity. It can be incorporated at desired positions within a peptide sequence to modulate the biological properties of the resulting peptide. The presence of the amino group on the tyrosine side chain allows for further derivatization, making it a versatile tool in peptide engineering.Furthermore, H-Tyr(3-NH2)-OH.2HCl can also be utilized in the development of pharmaceuticals, bioconjugates, and biomaterials where precise control over the structure and properties of the molecules is essential. Its compatibility with solid-phase peptide synthesis methods makes it a preferred choice for researchers and chemists working in the field of drug discovery and peptide-based therapeutics.Overall, H-Tyr(3-NH2)-OH.2HCl is a valuable reagent for chemists and researchers involved in peptide synthesis and drug development, offering a range of possibilities for the modification and manipulation of peptide structures for various applications in the biomedical and pharmaceutical industries.