L-Tyrosine
Product introduction:
Co heating with sugars can produce the reaction between amino carbonyls to produce a special flavor. Tyrosine is the catalytic substrate of tyrosinase monophenolase function and the main raw material for the final formation of eumelanin and brown melanin. In the research and development of whitening cosmetics, the synthesis of tyrosinase structural analogues competing with tyrosine can also effectively inhibit the production of melanin. Eating foods containing tyrosine in patients with vitiligo can promote the formation of melanin and reduce the symptoms of vitiligo. The raw material of amino acid infusion and amino acid compound preparation is used as nutritional supplement. Treat poliomyelitis, nuclear encephalitis, hyperthyroidism and other diseases. It is also used as raw material for manufacturing diiodine tyrosine, dibromo tyrosine and L-dopa.
CASNo.: 60-18-4
Molecular formula: C9H11NO3
Solubility:
Tasteless, soluble in formic acid, insoluble in water, insoluble in ethanol and ethyl ether.
Quality standard: CP2010 ,AJI92,USP26,EP4
Physical and chemical properties:
Molecular weight: 181.20
Density: 1.456 melting point (℃)
Properties: L- crystallized from water, colorless to white mercerized acicular crystal or crystalline powder; D- crystallized from water is colorless crystal; DL - crystals crystallized from water are shiny acicular crystals. It is a non essential amino acid in animals.
Specific rotation: L-body: - 10.6 ° (C = 4.1mol/lhcl, 25 ℃); d-body: + 10.3 ℃ (C = 4.1mol/lhcl).
Purpose:
Amino acid API, food additives, cosmetics, chemical intermediates, feed, fertilizer and other industries.
Nutritional supplements. After the reaction of amino carbonyl group with sugars, special flavor substances can be produced. It can be used for tissue culture (L-tyrosine · 2Na · H2O), biochemical reagent and treatment of hyperthyroidism. It can also be used as food for the aged and children and plant foliar nutrition.
IUPAC
2-[1-(aminomethyl)cyclohexyl]acetic acid
SMILES
C1=CC(=CC=C1CC(C(=O)O)N)O