APROBARBITAL METHANOL SOLUTION
- Product Name
- APROBARBITAL METHANOL SOLUTION
- CAS No.
- 77-02-1
- Chemical Name
- APROBARBITAL METHANOL SOLUTION
- Synonyms
- Numal;Isonal;Aprozal;Allonal;Alurate;Allional;NSC120769;Aprobarbita;Allypropymal;Aprobarbitone
- CBNumber
- CB2497884
- Molecular Formula
- C10H14N2O3
- Formula Weight
- 210.23
- MOL File
- 77-02-1.mol
APROBARBITAL METHANOL SOLUTION Property
- Melting point:
- 140-141.5°
- Boiling point:
- 349.75°C (rough estimate)
- Density
- 1.2056 (rough estimate)
- refractive index
- 1.5000 (estimate)
- storage temp.
- 2-8°C
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 7.81±0.10(Predicted)
- color
- White to Off-White
- Water Solubility
- 4.121g/L(25 ºC)
Safety
- Hazard Codes
- F,T
- Risk Statements
- 11-23/25-36/38
- Safety Statements
- 16-24-45
- Hazardous Substances Data
- 77-02-1(Hazardous Substances Data)
- Toxicity
- LD50 i.p. in mice: 200 mg/kg (Frey)
- DEA Controlled Substances
- CSCN: 2100
CSA SCH: Schedule III
NARC: No
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H301Toxic if swalloed
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P321Specific treatment (see … on this label).
P330Rinse mouth.
P405Store locked up.
P501Dispose of contents/container to..…
APROBARBITAL METHANOL SOLUTION Chemical Properties,Usage,Production
Originator
Alurate,Roche
Uses
Controlled substance (depressant). Sedative, hypnotic.
Definition
ChEBI: A member of the class of barbiturates that is pyrimidine-2,4,6(1H,3H,5H)-trione substituted by an isopropyl and a prop-1-en-3-yl group at position 5.
Manufacturing Process
170 parts of isopropylbarbituric acid are mixed with 500 parts of water and dissolved by adding 135 parts of a 30 percent of the solution of sodium hydroxide. To this solution are added 130 parts of 130 parts of allylbromide. An emulsion obtained is stirred at an inner temperature of about 25°C. The reaction is at first accompanied by a slight development of heat. After 12 hours the reaction is brought to a close. When cooled down the isopropylallylbarbituric acid is drawn off. The yield is more than 80 percent of the theoretically calculated quantity. By crystallization from diluted alcohol the pure isopropylallylbarbituric acid is obtained in colorless crystals of the melting point 137-138°C.
Therapeutic Function
Sedative, Hypnotic
World Health Organization (WHO)
Aprobarbital is an intermediate-acting barbiturate. See WHO comment for barbiturates.