L-Tyrosine Methyl Ester
Nanjing Finechem Holdings Co., LTD
Specifications
N/A
Packing & Storage
Packing
Storage Powder -20°C 3 years 4°C 2 years;In solvent -80°C 6 months, -20°C 1 month
Shipping Room temperature in continental US; may vary elsewhere
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General Information
Chemical & Physical Properties
Safety Information
Synthetic Route
Biological Activity
Common Names H-Tyr-OMe
Structure
CAS No. 1080-06-4 Boiling Point (℃) 330.0±27.0 °C at 760 mmHg
Molecular Weight 195.215 Melting Point (℃) 134-136 °C(lit.)
Density 1.2±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C10H13NO3 Flash Point (℃) 153.4±23.7 °C
Solubility N/A Autoignition Temperature (℃) N/A
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes T+:Very toxic
Safety Phrases S1-S28-S45
RIDADR NONH for all modes of transport
WGK Germany  3
SYMPTOMS PREVENTION FIRST AID
Inhalation Cough. Sore throat. Use local exhaust or breathing protection. Fresh air, rest.
Skin Redness. Burning sensation. Itching. Protective gloves. Remove contaminated clothes. Rinse and then wash skin with water and soap.
Eyes Redness. Pain. Wear safety goggles. First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Ingestion Abdominal pain. Nausea. Vomiting. Do not eat, drink, or smoke during work. Wash hands before eating. Rinse mouth. Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Refer for medical attention.
Description H-Tyr-OMe, an amino acid, is an endogenous metabolite[1].
Target Human Endogenous Metabolite
In Vitro DL-Lysine (Lys) is a high affinity, basic amino acid substrate for amino acid transporter b0,+ with Km value ranging from 100-400 μM[1].
References [1]. B.Korbélya, et al. Amino acids and their Cu complexes covalently grafted onto a polystyrene resin-A vibrational spectroscopic study. Journal of Molecular Structure. Volumes 834-836, 27 May 2007, Pages 345-348.
Synonyms
MFCD00002392
L-TYROSINE, METHYL ESTER
Tyrosine, methyl ester
Tyrosine, methyl ester, L-
l-tyrosine methyl ester
EINECS 214-095-3
methyl (2S)-2-amino-3-(4-hydroxyphenyl)propanoate
Tyrosine methyl ester
Methyl tyrosinate
Methyl L-tyrosinate
H-TYR-OME
Product Description
Introduction: L-Tyrosine tert-Butyl Ester is a valuable compound with diverse applications in various industries. This product introduction aims to provide a comprehensive overview of L-Tyrosine tert-Butyl Ester, including its production process, wide-ranging applications, and promising market prospects. With its unique properties and increasing demand, L-Tyrosine tert-Butyl Ester is poised to be a valuable ingredient in the global market.

Production: L-Tyrosine tert-Butyl Ester is typically produced through a well-established chemical process. The production involves the reaction of L-tyrosine with tert-butyl alcohol in the presence of a catalyst, resulting in the formation of L-Tyrosine tert-Butyl Ester. The subsequent purification and quality control processes ensure the production of a high-purity and consistent-quality final product.

Applications: L-Tyrosine tert-Butyl Ester finds applications in diverse industries due to its unique properties:
a. Pharmaceutical Industry: L-Tyrosine tert-Butyl Ester is extensively used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical compounds. It serves as a precursor for the production of tyrosine-containing drugs, peptides, and other bioactive molecules. Its incorporation into pharmaceutical formulations can enhance drug stability, bioavailability, and target specificity.

b. Cosmetics Industry: L-Tyrosine tert-Butyl Ester is employed in the cosmetics industry for its skin-enhancing properties. It can be utilized in the formulation of skincare products aimed at brightening the complexion, reducing the appearance of dark spots, and promoting an even skin tone. Its antioxidant properties contribute to its potential as an anti-aging ingredient.

c. Research and Development: L-Tyrosine tert-Butyl Ester plays a significant role in chemical research and development. It serves as a versatile building block for the synthesis of novel compounds, dyes, and specialty chemicals. Its reactivity and compatibility with various functional groups make it an important tool for the development of innovative products.

Market Prospects: L-Tyrosine tert-Butyl Ester demonstrates promising market prospects due to the following factors:
a. Growing Pharmaceutical Industry: The continuous growth of the global pharmaceutical industry and the demand for novel drug compounds drive the market for L-Tyrosine tert-Butyl Ester. Its role as a key intermediate in pharmaceutical synthesis and its potential applications in drug formulation make it a valuable component in the industry.

b. Rising Demand in Cosmetics Industry: The cosmetics industry's focus on innovative and effective skincare products creates a favorable market environment for L-Tyrosine tert-Butyl Ester. Its skin-enhancing properties and potential anti-aging effects contribute to its market growth.

c. Research and Development Opportunities: The need for versatile building blocks and intermediates in chemical research and development contributes to the market prospects of L-Tyrosine tert-Butyl Ester. Its reactivity and versatility make it a valuable tool for the development of new compounds and materials.

Conclusion: L-Tyrosine tert-Butyl Ester is a versatile compound with significant production, diverse applications, and promising market prospects. Its role in the pharmaceutical industry, cosmetics sector, and chemical research highlights its wide-ranging utility. With the growing demand for novel drug compounds, skincare innovations, and versatile building blocks in chemical synthesis, L-Tyrosine tert-Butyl Ester is expected to experience substantial growth in the global market. Manufacturers and industries can leverage its unique properties to develop advanced products and formulations to meet evolving market demands.

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