CBZ-D-tryptophan
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 Z-D-Trp-OH
Structure
CAS No. 2279-15-4 Boiling Point (℃) 619.1±55.0 °C at 760 mmHg
Molecular Weight 338.357 Melting Point (℃) 122-124°C
Density 1.3±0.1 g/cm3 Vapor Specific Gravity N/A
Molecular Formula C19H18N2O4 Flash Point (℃) 328.2±31.5 °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 DL-Lysine (Lysine) is an α-amino acid that is used in the biosynthesis of proteins.
Target Km: 100-400 μM (amino acid transporter b0,+)[1]
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]. Nguyen TV, et al. PEPT1 enhances the uptake of gabapentin via trans-stimulation of b0,+ exchange. Pharm Res. 2007 Feb;24(2):353-60.
Synonyms
Nalpha-Cbz-D-tryptophan
N-[(Benzyloxy)carbonyl]-D-tryptophan
Z-D-Trp-OH
Cbz-D-Trp-OH
Nα-Cbz-D-tryptophan
N-[(Benzyloxy)carbonyl]tryptophan
CBZ-D-TRYPTOPHAN
benzyloxycarbonyltryptophan
D-Tryptophan, N-[(phenylmethoxy)carbonyl]-
Nα-Carbobenzoxy-D-tryptophan
N-Cbz-D-Trp
MFCD00037945
N-Cbz-D-Tryptophan
2-{[(Benzyloxy)carbonyl]amino}-3-(1H-indol-3-yl)propanoic acid
Tryptophan, N-[(phenylmethoxy)carbonyl]-
Nalpha-Carbobenzoxy-D-tryptophan
(R)-2-(((Benzyloxy)carbonyl)amino)-3-(1H-indol-3-yl)propanoic acid
Product Description
CBZ-D-Tryptophan is an innovative chemical compound specifically designed to provide exceptional protection for amino acids during various chemical processes. With its unique properties and wide-ranging applications in the field of chemical synthesis, CBZ-D-Tryptophan has gained significant recognition in the global market. This product introduction aims to highlight the key features, benefits, and potential applications of CBZ-D-Tryptophan, emphasizing its crucial role in safeguarding amino acids and enabling efficient synthesis in the ever-evolving chemical industry.

Advancements in Chemical Engineering: CBZ-D-Tryptophan represents a significant breakthrough in chemical engineering, characterized by exceptional stability and compatibility with diverse reaction conditions. Developed through extensive research and state-of-the-art manufacturing techniques, this compound offers superior protection for amino acids, ensuring their integrity and preventing undesired reactions during synthetic procedures.

Unparalleled Amino Acid Protection: CBZ-D-Tryptophan provides unparalleled protection for amino acids by forming a robust and reversible bond. This protective group effectively shields the amino acid moiety from unwanted interactions, preserving the reactivity of the functional groups. This precise control over chemical transformations enhances overall synthetic efficiency, facilitating the production of high-quality amino acid derivatives with excellent yield and purity. CBZ-D-Tryptophan streamlines downstream processing and reduces production costs.

Broad Applications in Chemical Synthesis: CBZ-D-Tryptophan finds extensive utility in various chemical synthesis applications due to its exceptional protective properties. It is widely used in peptide synthesis, the production of pharmaceutical intermediates, and the preparation of complex organic molecules. CBZ-D-Tryptophan exhibits compatibility with a diverse range of solvents and reagents, making it an ideal choice for both traditional and advanced synthetic methodologies.

Global Market Impact: In the highly competitive global chemical market, CBZ-D-Tryptophan has emerged as a leading solution. Its consistent quality, reliability, and cost-effectiveness have earned it a strong reputation among researchers, scientists, and industry professionals. The product has witnessed a significant surge in demand, attracting a growing customer base across different regions. CBZ-D-Tryptophan has become an essential tool for chemical manufacturers seeking to optimize their synthetic processes and deliver high-quality amino acid derivatives.

Conclusion: CBZ-D-Tryptophan revolutionizes amino acid protection in chemical synthesis, offering exceptional stability, compatibility, and reliability. Its broad applications and positive impact on the global market position it as a key component of modern chemical engineering. By choosing CBZ-D-Tryptophan, 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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