H-Gly(Propargyl)-OH.HCl
L-Propargylglycine
CAS: 198774-27-5
Molecular Formula: C5H7NO2
H-Gly(Propargyl)-OH.HCl - Names and Identifiers
H-Gly(Propargyl)-OH.HCl - Physico-chemical Properties
| Molecular Formula | C5H7NO2 |
| Molar Mass | 113.11 |
| Boling Point | 273.5℃ at 760 mmHg |
| Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
H-Gly(Propargyl)-OH.HCl - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 10 |
H-Gly(Propargyl)-OH.HCl - Introduction
L-Propargylglycine is an organic compound that contains propargyl and glycine groups in its chemical structure. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: The L-Propargylglycine is white crystalline powder.
-Solubility: It is difficult to dissolve in water, but it is soluble in some organic solvents such as alcohols and ketones.
Use:
-Biological research: L-Propargylglycine can be used as a substrate to inhibit glycine aminase, thereby preventing glycine metabolism, and then controlling the formation of collagen. It plays an important role in the study of cell growth and the synthesis of extracellular matrix.
Preparation Method:
-The preparation method of L-Propargylglycine can be obtained by reaction. A common method is to esterify propargylamine with L-glycine to form the L-Propargylglycine esterification product, which is then hydrolyzed by acid or enzymatic hydrolysis to obtain the final product.
Safety Information:
- L-Propargylglycine has not been extensively studied, so data on its safety are limited. Appropriate laboratory safety measures, such as wearing gloves and goggles, should be taken during use or handling.
-Due to its chemical properties, it may cause irritation to the eyes, skin and respiratory system, so rinse with plenty of water immediately after contact. If discomfort occurs, consult a doctor.
Nature:
-Appearance: The L-Propargylglycine is white crystalline powder.
-Solubility: It is difficult to dissolve in water, but it is soluble in some organic solvents such as alcohols and ketones.
Use:
-Biological research: L-Propargylglycine can be used as a substrate to inhibit glycine aminase, thereby preventing glycine metabolism, and then controlling the formation of collagen. It plays an important role in the study of cell growth and the synthesis of extracellular matrix.
Preparation Method:
-The preparation method of L-Propargylglycine can be obtained by reaction. A common method is to esterify propargylamine with L-glycine to form the L-Propargylglycine esterification product, which is then hydrolyzed by acid or enzymatic hydrolysis to obtain the final product.
Safety Information:
- L-Propargylglycine has not been extensively studied, so data on its safety are limited. Appropriate laboratory safety measures, such as wearing gloves and goggles, should be taken during use or handling.
-Due to its chemical properties, it may cause irritation to the eyes, skin and respiratory system, so rinse with plenty of water immediately after contact. If discomfort occurs, consult a doctor.
Last Update：2024-04-09 21:04:16
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Spot supply
Product Name: (S)-2-Aminopent-4-ynoic acid hydrochloride Visit Supplier Webpage Request for quotationCAS: 198774-27-5
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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