Barbital Barbital

Barbiturate structural formula

Structural formula

Business number 018M
Molecular formula C8H12N2O3
Molecular weight 184.19
label

5,5-diethylbarbituric acid,

5,5-Diethyl-2,4,6(1H,3H,5H)-pyrimidinetrione,

5,5-Diethylbarbituric acid,

Barbitone,

Veronal

Numbering system

CAS number:57-44-3

MDL number:MFCD00036212

EINECS number:200-331-2

RTECS number:CQ3500000

BRN number:163999

PubChem number:24891513

Physical property data

1. Characteristics: White Needle crystalline or crystalline powder. Odorless. Slightly bitter. Sublime in a vacuum.


2. Density ( g/mL,25/4): Undetermined


3. Relative vapor density (g/mL,air=1): Undetermined


4. Melting point ( ºC): 188192


5. Boiling point ( ºC,Normal pressure): Undetermined


6. Boiling point ( ºC,5.2kPa): Undetermined


7. Refractive Index: Undetermined


8. Flashpoint (ºC): Undetermined


9. Specific optical rotation (º): Undetermined


10. Autoignition point or ignition temperature (ºC): Not OK


11. Vapor pressure (kPa,25ºC): Undetermined


12. Saturation vapor pressure (kPa,60ºC): Undetermined Molar volume (m3/mol):161.5


3. isotonic specific volume (90.2K):389.1


4. Surface Tension (dyne/cm):33.6


5. Polarizability10-24cm3):17.47

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 5

6. Topological molecule polar surface area 75.3

7. Number of heavy atoms: 13

8. Surface charge: 0

9. Complexity: 247

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

This product should be kept sealed.

Synthesis method

diethyl malonate is obtained by ethylation, cyclization and acidification.

Purpose

Prepare buffer solution. Protein electrophoresis. Liver function tests. Hydrogen peroxide stabilizer.

This product can be used as a hypnotic. Due to safety, effectiveness and drug resistance caused by repeated use, the use of barbiturates as hypnotic drugs has tended to decrease. Barbiturate tablets were released by the Department of Health1982year9One ​​of the eliminated drugs announced in March. Barbiturates can be used as hydrogen peroxide stabilizers; used in the preparation of buffer solutions, protein electrophoresis, liver function testing, etc.

oma”>Diethyl malonate is obtained by ethylation, cyclization and acidification.

Purpose

Prepare buffer solution. Protein electrophoresis. Liver function tests. Hydrogen peroxide stabilizer.

This product can be used as a hypnotic. Due to safety, effectiveness and drug resistance caused by repeated use, the use of barbiturates as hypnotic drugs has tended to decrease. Barbiturate tablets were released by the Department of Health1982year9One ​​of the eliminated drugs announced in March. Barbiturates can be used as hydrogen peroxide stabilizers; used in the preparation of buffer solutions, protein electrophoresis, liver function testing, etc.

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/22250

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