AZOBENZENE-D10
AZOBENZENE-D10
CAS: 30504-49-5
Molecular Formula: C12D10N2
AZOBENZENE-D10 - Names and Identifiers
| Name | AZOBENZENE-D10 |
| Synonyms | AZOBENZENE-D10 |
| CAS | 30504-49-5 |
AZOBENZENE-D10 - Physico-chemical Properties
| Molecular Formula | C12D10N2 |
| Molar Mass | 192.28 |
AZOBENZENE-D10 - Introduction
AZOBENZENE-D10(Azobenzene-D10) is an azobenzene compound labeled with deuterium (D). Its chemical formula is C12D10N2 and its relative molecular mass is 190.31g/mol.
AZOBENZENE-D10 is an organic molecule with two benzene rings in which one hydrogen atom is replaced by deuterium. Because its molecular structure contains nitrogen-nitrogen double bonds, it has good light response characteristics. Under the irradiation of ultraviolet light, the AZOBENZENE-D10 can undergo photoisomerization reaction, that is, the molecular structure can be changed from cis-cis (trans) to trans-trans (cis). This process of photoisomerization is reversible and can be converted to cis-CIS structure again by light or heat treatment.
One of the main uses of AZOBENZENE-D10 is as a photosensitive dye in optical devices such as fluorescence microscopy, laser printing, and optical switches. It can also be used to study the properties and applications of photoresponsive materials, as well as labeling reagents for Analytical Chemistry.
The method of preparing the AZOBENZENE-D10 includes introducing a deuterated reagent to replace the amino group or hydrogen atom during the synthesis. Methods can vary depending on the specific chemical reaction conditions, but typically use sodium deuteride (NaD) or other deuterating reagents to react with azobenzene.
Regarding the safety information of AZOBENZENE-D10, it is an organic compound that may have certain risks to the human body and the environment. In use and operation, should follow the relevant safety procedures. Direct contact with skin and eyes should be avoided and good ventilation should be maintained. If exposed or inhaled, wash off immediately or seek medical advice. In addition, AZOBENZENE-D10 is also a combustible material, should be away from the fire and high temperature environment.
Before purchasing and using AZOBENZENE-D10, it is recommended to consult a professional or chemical supplier for more detailed information and guidance.
AZOBENZENE-D10 is an organic molecule with two benzene rings in which one hydrogen atom is replaced by deuterium. Because its molecular structure contains nitrogen-nitrogen double bonds, it has good light response characteristics. Under the irradiation of ultraviolet light, the AZOBENZENE-D10 can undergo photoisomerization reaction, that is, the molecular structure can be changed from cis-cis (trans) to trans-trans (cis). This process of photoisomerization is reversible and can be converted to cis-CIS structure again by light or heat treatment.
One of the main uses of AZOBENZENE-D10 is as a photosensitive dye in optical devices such as fluorescence microscopy, laser printing, and optical switches. It can also be used to study the properties and applications of photoresponsive materials, as well as labeling reagents for Analytical Chemistry.
The method of preparing the AZOBENZENE-D10 includes introducing a deuterated reagent to replace the amino group or hydrogen atom during the synthesis. Methods can vary depending on the specific chemical reaction conditions, but typically use sodium deuteride (NaD) or other deuterating reagents to react with azobenzene.
Regarding the safety information of AZOBENZENE-D10, it is an organic compound that may have certain risks to the human body and the environment. In use and operation, should follow the relevant safety procedures. Direct contact with skin and eyes should be avoided and good ventilation should be maintained. If exposed or inhaled, wash off immediately or seek medical advice. In addition, AZOBENZENE-D10 is also a combustible material, should be away from the fire and high temperature environment.
Before purchasing and using AZOBENZENE-D10, it is recommended to consult a professional or chemical supplier for more detailed information and guidance.
Last Update：2024-04-10 22:29:15
