Cas no 303-95-7 (Coenzyme Q7)
Coenzyme Q7 Chemical and Physical Properties
Names and Identifiers
-
- 2,5-Cyclohexadiene-1,4-dione,2-[(2E,6E,10E,14E,18E,22E)-3,7,11,15,19,23,27-heptamethyl-2,6,10,14,18,22,26-octacosaheptaen-1-yl]-5,6-dimethoxy-3-methyl-
- Coenzyme Q7
- 2-[(2E,6E,10E,14E,18E,22E)-3,7,11,15,19,23,27-Heptamethyl-2,6,10, 14,18,22,26-octacosaheptaen-1-yl]-5,6-dimethoxy-3-methyl-1,4-benz oquinone
- All-Trans Coenzyme Q7
- Carenone
- Coenz10
- coenzyme Q10
- COQ10
- eiquinon
- Ensorb
- Kudesan
- Liquid-Q
- neuqinon
- oxidized coenzyme Q10
- oxidized coenzyme Q7
- Q-10
- Q-Gel
- trans-Ubichinon-7
- Ubichinon-35
- ubiquinone Q10
- ubiquinone-35
- UNII-RRK47DEG6Q
- Ubiquinone 7
- 2-[(2E,6E,10E,14E,18E,22E)-3,7,11,15,19,23,27-heptamethyloctacosa-2,6,10,14,18,22,26-heptaenyl]-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
- NSC-147790
- NSC147790
- (all-E)-2-(3,7,11,15,19,23,27-heptamethyl-2,6,10,14,18,22,26-octacosaheptenyl)-5,6-dimethoxy-3-methyl-2,5-cyclohexadiene-1,4-dione
- CHEBI:46448
- COQ7
- 4-08-00-03295 (Beilstein Handbook Reference)
- Ubiquinone 35
- 2,3-dimethoxy-5-methyl-6-heptaprenyl-1,4-benzoquinone
- 25222-34-8
- 2-((2E,6E,10E,14E,18E,22E)-3,7,11,15,19,23,27-Heptamethyloctacosa-2,6,10,14,18,22,26-heptaen-1-yl)-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
- ubiquinone(7)
- 2-[(2E,6E,10E,14E,18E,22E)-3,7,11,15,19,23,27-heptamethyloctacosa-2,6,10,14,18,22,26-heptaen-1-yl]-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
- 2-(3,7,11,15,19,23,27-heptamethyloctacosa-2,6,10,14,18,22,26-heptaenyl)-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
- 2-[(2E,6E,10E,14E,18E,22E)-3,7,11,15,19,23,27-heptamethyloctacosa-2,6,10,14,18,22,26-heptaen-1-yl]-5,6-dimethoxy-3-methyl-1,4-benzoquinone
- trans-Coenzyme Q7
- UBIQUINONE-7 [JAN]
- Q27120651
- 2,5-Cyclohexadiene-1,4-dione, 2-(3,7,11,15,19,23,27-heptamethyl-2,6,10,14,18,22,26-octacosaheptenyl)-5,6-dimethoxy-3-methyl-, (all-E)-
- DTXSID501318261
- 2-((2E,6E,10E,14E,18E,22E)-3,7,11,15,19,23,27-heptamethyl-2,6,10,14,18,22,26-octacosaheptaenyl)-5,6-dimethoxy-3-methyl-2,5-cyclohexadiene-1,4-dione
- UBIDECARENONE IMPURITY B [EP IMPURITY]
- 2,5-Cyclohexadiene-1,4-dione, 2-((2E,6E,10E,14E,18E,22E)-3,7,11,15,19,23,27-heptamethyl-2,6,10,14,18,22,26-octacosaheptaenyl)-5,6-dimethoxy-3-methyl-
- coenzyme-Q7
- UQ7
- 303-95-7
- UBIQUINONE-7
- RRK47DEG6Q
- BRN 2406878
- Ubiquinone Q7
-
- Inchi： 1S/C44H66O4/c1-32(2)18-12-19-33(3)20-13-21-34(4)22-14-23-35(5)24-15-25-36(6)26-16-27-37(7)28-17-29-38(8)30-31-40-39(9)41(45)43(47-10)44(48-11)42(40)46/h18,20,22,24,26,28,30H,12-17,19,21,23,25,27,29,31H2,1-11H3/b33-20+,34-22+,35-24+,36-26+,37-28+,38-30+
- InChI Key： DBESHHFMIFSNRV-RJYQSXAYSA-N
- SMILES： O(C)C1=C(C(C(C)=C(C1=O)C/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/C)=O)OC
Computed Properties
- Exact Mass: 658.49600
- Monoisotopic Mass: 658.496
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 48
- Rotatable Bond Count: 22
- Complexity: 1360
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 6
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 52.6A^2
- XLogP3: 13.8
Experimental Properties
- Density: 1.0±0.1 g/cm3
- Melting Point: Not available
- Boiling Point: 736.9±60.0 °C at 760 mmHg
- Flash Point: 290.9±32.9 °C
- Refractive Index: 1.522
- PSA: 52.60000
- LogP: 12.67440
- Vapor Pressure: 0.0±2.4 mmHg at 25°C
Coenzyme Q7 Security Information
- Signal Word：warning
- Hazard Statement： H303+H313+H333
- Warning Statement： P264+P280+P305+P351+P338+P337+P313
- Safety Instruction： H303+H313+H333
- Storage Condition：storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
Coenzyme Q7 Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | C636480-10mg |
Coenzyme Q7 |
303-95-7 | 10mg |
$37161.00 | 2023-05-18 | ||
| BAI LING WEI Technology Co., Ltd. | J60C636480-25mg |
303-95-7 | 25mg |
￥350207 | 2025-07-04 |
Coenzyme Q7 Related Literature
-
Qin-Li Wan,Xiaodie Fu,Xiao Meng,Zhenhuan Luo,Wenyu Dai,Jing Yang,Chongyang Wang,Hao Wang,Qinghua Zhou Food Funct. 2020 11 347
Additional information on Coenzyme Q7
The Comprehensive Guide to Coenzyme Q7 (CAS No. 303-95-7): Properties, Applications, and Market Insights
Coenzyme Q7, also known as Ubiquinone-7, is a vital compound in the Coenzyme Q family, with the CAS number 303-95-7. This naturally occurring molecule plays a crucial role in cellular energy production and antioxidant defense. In recent years, Coenzyme Q7 supplements have gained popularity due to their potential health benefits, especially in anti-aging and energy metabolism.
The chemical structure of Coenzyme Q7 consists of a benzoquinone core with a seven-unit isoprenoid side chain, distinguishing it from other members like Coenzyme Q10. This structural difference affects its solubility and bioavailability, making CoQ7 particularly interesting for researchers studying mitochondrial function and cellular health.
One of the most searched questions about Coenzyme Q7 is "How does CoQ7 differ from CoQ10?" While both compounds function as electron carriers in the mitochondrial respiratory chain, CoQ7 has shown unique properties in certain biochemical pathways. Recent studies suggest it may have specific advantages in supporting cardiovascular health and neurological function, though more research is needed.
The global market for Coenzyme Q7 products has been growing steadily, driven by increasing consumer awareness of nutritional supplements and healthy aging. Many users search for "best CoQ7 supplements" or "CoQ7 dosage recommendations," reflecting the compound's popularity in the wellness industry. Manufacturers are responding with innovative formulations that enhance CoQ7 absorption and bioavailability.
In the cosmetic industry, Coenzyme Q7 has emerged as a promising ingredient for anti-aging skincare products. Its antioxidant properties help combat free radical damage, a major contributor to skin aging. This application has made CoQ7 a trending topic in dermatological research and cosmeceutical development.
From a biochemical perspective, Coenzyme Q7 participates in the electron transport chain, facilitating ATP production. This fundamental role in cellular energy production explains why researchers are investigating its potential in addressing mitochondrial disorders and age-related energy decline.
The production of Coenzyme Q7 typically involves sophisticated fermentation technology or chemical synthesis methods. Quality control is essential, as purity significantly affects the compound's efficacy. Many consumers search for "pharmaceutical grade CoQ7" or "pure Coenzyme Q7 powder," indicating demand for high-quality products.
Recent scientific literature highlights potential applications of CoQ7 in supporting cognitive function and neuroprotection. Some studies suggest it may help maintain brain health by protecting neurons from oxidative stress, making it a subject of interest in neurological research.
When considering Coenzyme Q7 supplementation, it's important to understand factors affecting its bioavailability. Formulations with enhanced delivery systems, such as liposomal CoQ7 or water-soluble CoQ7, are becoming increasingly popular among health-conscious consumers.
The regulatory status of Coenzyme Q7 varies by region, but it's generally recognized as safe when used appropriately. However, questions like "Is CoQ7 FDA approved?" or "CoQ7 side effects" remain common among first-time users, emphasizing the need for clear, science-based information.
Future research directions for Coenzyme Q7 include exploring its potential in metabolic syndrome management and as an adjunct in therapeutic protocols. The compound's unique properties continue to attract scientific interest, particularly in the context of personalized nutrition and preventive healthcare strategies.
For formulators and product developers, understanding the stability of CoQ7 in various matrices is crucial. The compound's sensitivity to heat and light requires careful consideration during product development, especially for functional foods and beverage applications.
In conclusion, Coenzyme Q7 (CAS 303-95-7) represents an important member of the ubiquinone family with distinct properties and potential applications. As research continues to uncover its benefits, we can expect growing interest in this compound from both the scientific community and health-conscious consumers worldwide.
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