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N-Boc-N’-(2-chlorobenzyloxycarbonyl)-L-lysine(CAS# 54613-99-9)

Chemical Property:

Molecular Formula C19H27ClN2O6
Molar Mass 414.88
Density 1.236±0.06 g/cm3(Predicted)
Melting Point 70-73°C
Boling Point 608.3±55.0 °C(Predicted)
Flash Point 321.7°C
Vapor Presure 1.19E-15mmHg at 25°C
Appearance Crystallization
Color White to off-white
pKa 3.99±0.21(Predicted)
Storage Condition Sealed in dry,2-8°C
Refractive Index 1.531
MDL MFCD00038386
Physical and Chemical Properties N-tert-butoxycarbonyl-N’-(2-chlorobenzyloxycarbonyl)-L-lysine is white to off-white powder in appearance; melting point 70-73°C; density 1.236g/cm3.
Use Protected lysine is particularly suitable for solid-phase peptide synthesis; 2-CZ protection is about 50 times more stable than Z-group protection.

Product Detail

Product Tags

Hazard Symbols Xi – Irritant
Risk Codes 36/37/38 – Irritating to eyes, respiratory system and skin.
Safety Description S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 – Wear suitable protective clothing.
S24/25 – Avoid contact with skin and eyes.
WGK Germany 3
HS Code 29242990

 

Introduction

N-tert-butoxycarbonyl-N’-(2-chlorobenzyloxycarbonyl)-L-lysine is an organic compound, commonly referred to as CBZ-L-lysine. The following is the nature, use, preparation method and safety information of the compound:

 

Quality:

CBZ-L-lysine is a colorless crystalline solid with a peculiar odor. It has good solubility and is soluble in common organic solvents such as methanol, chloroform, and dimethyl sulfoxide.

 

Use:

CBZ-L-lysine is often used as one of the amino protective groups in organic synthesis to protect the amino functional groups that are sensitive to the environment. In the synthesis of peptide compounds, CBZ-L-lysine can be used to protect the amino group of lysine in order to protect or control its reactivity in specific reactions.

 

Method:

The preparation of CBZ-L-lysine is usually carried out by the following steps: L-lysine is reacted with carbon dioxide to obtain the corresponding carbonate; Then, the carbonate is reacted with tert-butoxycarbonyl magnesium chloride to obtain acetyl-protected lysine; It is then reacted with 2-chlorobenzyl iodine chloride and alkali to obtain CBZ-L-lysine.

 

Safety Information:

The use of CBZ-L-lysine should be accompanied by the following safety precautions: it may be irritating to the eyes, skin and respiratory tract, and direct contact should be avoided during operation. Appropriate protective equipment such as chemical protective glasses and gloves should be worn during use. It should be operated in a well-ventilated area to avoid inhaling vapors from the compound. If an accident occurs, the affected area should be rinsed immediately with plenty of water and medical assistance should be sought.


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