Basic information
- Name:
Ubidecarenone
- CAS No.:
303-98-0
- Molecular Structure:

- Formula:
- C59H90O4
- Molecular Weight:
- 863.49
- Deleted CAS:
- 13448-14-1|55870-43-4
- Synonyms:
- Terekol;Heartcin;Udekinon Emitolon;Ensorb;Ubiquinone 10;Ubiquinone 10 (Coenzyme Q10);Udekinon;Co Q10;CoQ10;Ubiquinone 50;Bio-Quinon;Q 199;Inokiten;Coenzyme Q10;Neuquinone;Q 10;2,5-Cyclohexadiene-1,4-dione,2-[(2E,6E,10E,- 14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,- 31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,- 38-tetracontadecaenyl]-5,6-dimethoxy-3- methyl-;Water soluble coenzyme Q10;Ubidecarenone (Coenzyme Q10) USP28;CO-Q10;Coenzyme Q10(Ubiquinone);Ubidecarenone Coenzyme Q10;Ube-Q;Adelir;Coezime Q10;
- EINECS:
- 206-147-9
- Density:
- 0.97 g/cm3
- Melting Point:
- 49-51 °C
- Boiling Point:
- 869 °C at 760 mmHg
- Flash Point:
- 324.5 °C
- Appearance:
- yellow-orange crystalline powder
- Hazard Symbols:
Xi- Risk Codes:
- 36/37/38
- Safety Description:
- 22-24/25-26 Details
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Chemistry
Molecule structure of Ubidecarenone (CAS NO.303-98-0):
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IUPAC Name: 2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-Decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
Molecular Weight: 863.3435 g/mol
Molecular Formula: C59H90O4
Density: 0.97 g/cm3
Melting Point: 49-51 °C
Boiling Point: 869 °C at 760 mmHg
Flash Point: 324.5 °C
Index of Refraction: 1.525
Molar Refractivity: 272.64 cm3
Molar Volume: 888.5 cm3
Surface Tension: 38.5 dyne/cm
Enthalpy of Vaporization: 126.29 kJ/mol
Vapour Pressure: 1.23E-30 mmHg at 25 °C
Storage Temp. −20 °C
Stability: stable, but may be light or heat sensitive. Incompatible with strong oxidizing agents.
XLogP3-AA: 19.4
H-Bond Acceptor: 4
Rotatable Bond Count: 31
Heavy Atom Count: 63
InChIKey: ACTIUHUUMQJHFO-UPTCCGCDSA-N
EINECS: 206-147-9
Product Categories: Drug bulk;Mixed Fatty Acids;Antioxidant;Benzoquinones;Biochemistry;Vitamin Related Compounds;Vitamins;Nutritional Supplements;Drugs & Medication;Fatty Acid Derivatives & Lipids;Glycerols;Steroids
History
In 1957, Ubidecarenone was first discovered by Professor Fredrick L. Crane and colleagues at the University of Wisconsin–Madison Enzyme Institute. Its chemical structure was reported by Dr. Karl Folkers and coworkers at Merck in 1958; in 1968, Folkers became a Professor in the Chemistry Department at the University of Texas at Austin.
Uses
Ubidecarenone (CAS NO.303-98-0) can be widely used as antibacterial, antioxidant agent in food, cosmetics, dietary supplements industry.
Toxicity Data With Reference
| 1. | orl-mus TDLo:42 mg/kg (female 7-13D post):REP | IYKEDH Iyakuhin Kenkyu. Study of Medical Supplies. 3 (1972),306. | ||
| 2. | orl-mus TDLo:4200 mg/kg (female 7-13D post):TER | IYKEDH Iyakuhin Kenkyu. Study of Medical Supplies. 3 (1972),306. | ||
| 3. | orl-rat LDLo:4000 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),862. | ||
| 4. | scu-rat LDLo:500 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),862. | ||
| 5. | ivn-rat LDLo:250 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),862. | ||
| 6. | ims-rat LDLo:500 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),862. | ||
| 7. | orl-mus LDLo:4000 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),862. | ||
| 8. | scu-mus LDLo:500 mg/kg | NIIRDN “Drugs in Japan. Ethical Drugs, 6th Edition 1982“ Edited by Japan Pharmaceutical Information Center. 6 (1982),862. | ||
| 9. | ivn-mus LDLo:500 mg/kg |
Consensus Reports
Reported in EPA TSCA Inventory.
Safety Profile
Hazard Codes:
Xi
Risk Statements: 36/37/38
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 22-24/25-26
S22:Do not breathe dust.
S24/25:Avoid contact with skin and eyes.
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany: 3
RTECS: DK3900000
F: 8-10
Poison by intravenous route. Moderately toxic by ingestion, subcutaneous, and intramuscular routes. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits acrid smoke and irritating fumes.
Specification
Ubidecarenone (CAS NO.303-98-0) is also named as 2,5-Cyclohexadiene-1,4-dione, 2-((2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl)-5,6-dimethoxy-3-methyl ; CCRIS 9016 ; Co Q10 ; Co-enzyme Q-10 ; CoQ 10 ; CoQ(sub 10) ; Coenzyme Q ; Coenzyme Q 10 ; Luvacor ; Mitoquinone ; NSC 140665 ; NSC 140865 ; Neuquinon ; Neuquinone ; Q 199 ; Terekol ; UNII-EJ27X76M46 ; Ubidecarenonum ; Ubidecarenonum [Latin] ; Ubiquinone 10 ; Ubiquinone 50 ; Ubiquinone (sub 10) ; Udekinon . Ubidecarenone (CAS NO.303-98-0) is yellow-orange crystalline powder.

