3-Indoxyl-beta-D-galactopyranoside - Names and Identifiers
3-Indoxyl-beta-D-galactopyranoside - Physico-chemical Properties
Molecular Formula | C14H17NO6
|
Molar Mass | 295.29 |
Density | 1.562g/cm3 |
Boling Point | 606.7°C at 760 mmHg |
Flash Point | 320.7°C |
Vapor Presure | 1.43E-15mmHg at 25°C |
Appearance | White to off-white powder |
Storage Condition | 2-8°C |
Refractive Index | 1.715 |
MDL | MFCD00083389 |
Physical and Chemical Properties | Storage Conditions: 2-8 ℃ |
3-Indoxyl-beta-D-galactopyranoside - Risk and Safety
Risk Codes | 67 - Vapors may cause drowsiness and dizziness
|
Safety Description | 24/25 - Avoid contact with skin and eyes.
|
UN IDs | UN 3175 4.1 / PGII |
WGK Germany | 3 |
HS Code | 29349990 |
3-Indoxyl-beta-D-galactopyranoside - Introduction
3-Indolyl-beta-D-galactopyranoside is an organic compound with the chemical formula C14H17NO6. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 3-Indolyl-beta-D-galactopyranoside is a white to light yellow solid.
-Solubility: Its solubility in water is low, but it can be dissolved in some organic solvents, such as methanol and alcohol.
-Stability: Under dry, cool and sealed conditions, 3-indolyl-beta-D-galactopyranoside is relatively stable.
Use:
3-Indolyl-beta-D-galactopyranoside has a wide range of applications:
-Pharmaceutical field: It is used as a starting material for research and synthesis of compounds, and can also be used as a potential drug molecular skeleton.
-Biochemistry: 3-Indolyl-beta-D-galactopyranoside can be used to study the qualitative and quantitative nature of enzyme-linked immunosorbent assay (ELISA).
-Chemical synthesis: In organic synthesis, it can be used to synthesize complex natural products or other organic compounds.
Method:
Common methods for preparing 3-indolyl-beta-D-galactopyranoside include enzymatic methods and chemical synthesis methods. Among them, the enzymatic method is obtained by reacting glucopyranose and an indolyl structural compound under appropriate conditions by catalyzing a reaction using a glucopyranose transferase (glucosyltransferase). The chemical synthesis method is synthesized by a series of organic synthesis reaction steps.
Safety Information:
There are few safety and toxicity data on 3-indolyl-beta-D-galactopyranoside, so the following should be noted when using:
-Avoid swallowing, inhaling or touching skin and eyes. Personal protective equipment such as lab gloves, safety glasses and lab coats should be worn during operation.
-Store away from fire and high temperature and keep dry. Avoid prolonged exposure to air.
-Before use and disposal, the relevant safety data sheet and instructions for use should be read and followed.
Please conduct a safety assessment before use, and conduct appropriate laboratory operations and waste disposal.
Last Update:2024-04-09 21:54:55