N-acetyl-L-tyrosine
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
Free Quote
For samples, pricing, or more information, please call us at 0086-25-52397805 or mail to info@alchemist-chem.com or fill out the following form.
We will respond to you as soon as possible.

Tel: 0086-25-52397805

Email: info@alchemist-chem.com

General Information
Chemical & Physical Properties
Safety Information
Synthetic Route
Biological Activity
Common Names N-Acetyl-L-tyrosine
Structure
CAS No. 537-55-3 Boiling Point (℃) 531.3±45.0 °C at 760 mmHg
Molecular Weight 223.225 Melting Point (℃) 149-152 °C(lit.)
Density 1.3±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C11H13NO4 Flash Point (℃) 275.1±28.7 °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 N-Acetyl-L-tyrosine originates from tyrosine through an AA acetylase, is associated with aromatic L-amino acid decarboxylase deficiency and tyrosinemia I.
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]. Abdenur JE, et al. Aromatic l-aminoacid decarboxylase deficiency: unusual neonatal presentation and additional findings in organic acid analysis. Mol Genet Metab. 2006 Jan;87(1):48-53.
Synonyms
(2S)-2-(acetylamino)-3-(4-hydroxyphenyl)propanoic acid
L-Tyrosine, N-acetyl-
Ac-L-Tyr-OH
acetyl tyrosine
N-AC-L-TYR
(2S)-2-acetamido-3-(4-hydroxyphenyl)propanoic acid
N-Ac-Tyr
EINECS 208-671-3
n-acetyl-l-tyrosin
AC-TYR-OH
N-Acetyltyrosine
N-acetyl-L-Tyr
Ac-L-Tyrosine
Product Description
Introduction: N-Acetyl-L-tyrosine, commonly known as N-Acetyltyrosine or NAT, is a significant chemical compound with diverse applications in the chemical industry. This product introduction aims to provide an overview of N-Acetyl-L-tyrosine, covering its raw materials, production process, market trends, and the current status of amino acids in the industry.

Raw Materials: N-Acetyl-L-tyrosine is synthesized using L-tyrosine and acetic anhydride as the primary raw materials. L-tyrosine, a nonessential amino acid, serves as the precursor for N-Acetyl-L-tyrosine synthesis. Acetic anhydride provides the acetyl group necessary for acetylation.

Production Process: The production process of N-Acetyl-L-tyrosine involves the following steps:
Step 1: Esterification reaction - L-tyrosine is reacted with acetic anhydride in the presence of suitable catalysts and reaction conditions to form N-Acetyl-L-tyrosine. The reaction takes place in a solvent or under solid-state conditions, depending on the specific manufacturing process.

Step 2: Purification and refinement - The resulting N-Acetyl-L-tyrosine is purified and refined using techniques such as filtration, crystallization, and chromatography to achieve the desired level of purity.

Market Trends: The market demand for N-Acetyl-L-tyrosine has been steadily increasing due to its diverse applications across various industries. Here are some key market trends:
Pharmaceuticals: N-Acetyl-L-tyrosine is utilized in the pharmaceutical industry. It is used as an ingredient in the formulation of drugs targeting cognitive function, mood enhancement, and stress management. It is also employed in the development of dietary supplements.

Cosmetics and Personal Care: N-Acetyl-L-tyrosine finds applications in cosmetics and personal care products. It is used in skincare formulations due to its potential to improve skin tone, reduce hyperpigmentation, and support the production of melanin, the pigment responsible for skin and hair color.

Chemical Research: N-Acetyl-L-tyrosine serves as a valuable compound in chemical research. It is used as a building block in the synthesis of peptides, pharmaceutical intermediates, and specialty chemicals. Its unique structure and functional groups make it useful for diverse synthetic applications.

Current Status of Amino Acids: Amino acids play a crucial role in various sectors, including pharmaceuticals, food additives, animal nutrition, and agriculture. The demand for amino acids continues to grow due to their diverse applications and essential role in biological processes. Nonessential amino acids, such as L-tyrosine, are of particular importance as they can be synthesized by the human body but are also obtained from dietary sources.

Conclusion: N-Acetyl-L-tyrosine, derived from L-tyrosine, holds significant value in the chemical industry. Its production involves the combination of raw materials and precise manufacturing processes. The market demand for N-Acetyl-L-tyrosine is driven by its applications in pharmaceuticals, cosmetics, personal care, and chemical research. Amino acids, including L-tyrosine, continue to play a vital role in various industries, and N-Acetyl-L-tyrosine maintains its position as a valuable chemical compound with diverse applications.

Leave A Message
Leave A Message ×
If you are interested in our products and want to know more details,please leave a message here,we will reply you as soon as we can.