MOC-L-tert-leucine
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 Methoxycarbonyl-L-tert-leucine
Structure
CAS No. 162537-11-3 Boiling Point (℃) 320.9±25.0 °C at 760 mmHg
Molecular Weight 189.209 Melting Point (℃) 109ºC
Density 1.1±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C8H15NO4 Flash Point (℃) 147.9±23.2 °C
Solubility Soluble in ethyl acetate and methanol. 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 (S)-2-(Methoxycarbonylamino)-3,3-dimethylbutanoic acid is a leucine derivative[1].
Target Km: 100-400 μM (amino acid transporter b0,+)[1]
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.
Synonyms
(2S)-2-(methoxycarbonylamino)-3,3-dimethylbutanoic acid
N-(Methoxycarbonyl)-L-tert-leucine
N-(Methoxycarbonyl)-3-methyl-L-valine
L-Valine, N-(methoxycarbonyl)-3-methyl-
Methoxycarbonyl-L-tert-leucine
N-Methoxycarbonyl-L-tert-leucine
(S)-2-((Methoxycarbonyl)amino)-3,3-dimethylbutanoic acid
Product Description
MOC-L-tert-leucine is an innovative chemical compound designed to provide exceptional protection for amino acids during various chemical processes. With its remarkable properties and wide-ranging applications in the field of chemical synthesis, MOC-L-tert-leucine has gained significant traction in the global market. This product introduction aims to showcase the unique features, benefits, and potential applications of MOC-L-tert-leucine, emphasizing its role in safeguarding amino acids and enabling efficient synthesis in the ever-expanding chemical industry.

Advancements in Chemical Engineering: MOC-L-tert-leucine represents a breakthrough in chemical engineering, demonstrating outstanding stability and compatibility with diverse reaction conditions. Developed through rigorous research and cutting-edge manufacturing techniques, this compound offers superior protection for amino acids, effectively preventing undesired reactions and ensuring their integrity during synthetic procedures.

Unmatched Amino Acid Protection: MOC-L-tert-leucine provides unmatched protection for amino acids by forming a robust and reversible bond. This protective group shields the amino acid moiety from unwanted interactions, thereby safeguarding the reactive functional groups. This precise control over chemical transformations enhances overall synthetic efficiency and enables the production of amino acid derivatives with high yield and purity. MOC-L-tert-leucine facilitates downstream processing and reduces production costs.

Versatile Applications in Chemical Synthesis: Due to its exceptional protective properties, MOC-L-tert-leucine finds extensive utility in various chemical synthesis applications. It is commonly utilized in peptide synthesis, the production of pharmaceutical intermediates, and the preparation of complex organic molecules. The compatibility of MOC-L-tert-leucine with a wide range of solvents and reagents makes it a versatile choice for traditional and advanced synthetic methodologies.

Impact in the Global Market: In today's highly competitive global chemical market, MOC-L-tert-leucine has emerged as a game-changer. Its consistent quality, reliability, and cost-effectiveness have established its reputation among researchers, scientists, and industry professionals. The product has witnessed a significant surge in demand, attracting a growing customer base worldwide. MOC-L-tert-leucine has become an indispensable tool for chemical manufacturers aiming to optimize their synthetic processes and deliver high-quality amino acid derivatives.

Conclusion: MOC-L-tert-leucine revolutionizes amino acid protection in chemical synthesis, offering exceptional stability, compatibility, and reliability. Its extensive applications and positive impact on the global chemical market have positioned it as a key component of modern chemical engineering. By choosing MOC-L-tert-leucine, researchers and manufacturers can confidently protect amino acids, enhance synthetic efficiency, and accelerate the development of pharmaceuticals, agrochemicals, and other complex organic compounds.

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