EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes

ubiquinone-5
2,5-cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3,7,11,15,19-pentamethyl-2,6,10,14,18-eicosapentaenyl)-, (all-E)-

Supplier Sponsors

Name:2,3-dimethoxy-5-methyl-6-[(2E,6E,10E,14E)-3,7,11,15,19-pentamethylicosa-2,6,10,14,18-pentaenyl]cyclohexa-2,5-diene-1,4-dione
CAS Number: 4370-61-0Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J492.361H
Beilstein Number:2315703
MDL:MFCD00274412
XlogP3-AA:10.10 (est)
Molecular Weight:522.76930000
Formula:C34 H50 O4
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 3.411e-008 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Glentham Life Sciences
Ubiquinone-5
Santa Cruz Biotechnology
For experimental / research use only.
Ubiquinone-5
 
Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for ubiquinone-5 usage levels up to:
 not for fragrance use.
 
Recommendation for ubiquinone-5 flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :12832984
National Institute of Allergy and Infectious Diseases:Data
2,3-dimethoxy-5-methyl-6-[(2E,6E,10E,14E)-3,7,11,15,19-pentamethylicosa-2,6,10,14,18-pentaenyl]cyclohexa-2,5-diene-1,4-dione
Chemidplus:0004370610
 
References:
 2,3-dimethoxy-5-methyl-6-[(2E,6E,10E,14E)-3,7,11,15,19-pentamethylicosa-2,6,10,14,18-pentaenyl]cyclohexa-2,5-diene-1,4-dione
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):12832984
Pubchem (sid):310281548
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
HMDB (The Human Metabolome Database):Search
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 palm oil
Search PMC Picture
 
Synonyms:
 coenzyme Q5
2,5-cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3,7,11,15,19-pentamethyl-2,6,10,14,18-eicosapentaenyl)-, (all-E)-
(all-E)-2,3-dimethoxy-5-methyl-6-(3,7,11,15,19-pentamethyl-2,6,10,14,18-eicosapentaenyl)-2,5-cyclohexadiene-1,4-dione
2,3-dimethoxy-5-methyl-6-[(2E,6E,10E,14E)-3,7,11,15,19-pentamethylicosa-2,6,10,14,18-pentaenyl]cyclohexa-2,5-diene-1,4-dione
 ubiquinone 25
 ubiquinone 5
 

Articles:

PubMed:Effects of ubiquinone derivatives on the mitochondrial unselective channel of Saccharomyces cerevisiae.
PubMed:Prerequisites for ubiquinone analogs to prevent mitochondrial permeability transition-induced cell death.
PubMed:Ubiquinone analogs: a mitochondrial permeability transition pore-dependent pathway to selective cell death.
PubMed:Coenzyme Q(1) depletes NAD(P)H and impairs recycling of ascorbate in astrocytes.
PubMed:Hepatocyte metabolism of coenzyme Q1 (ubiquinone-5) to its sulfate conjugate decreases its antioxidant activity.
PubMed:Electrochemical properties of natural organic matter (NOM), fractions of NOM, and model biogeochemical electron shuttles.
PubMed:Three classes of ubiquinone analogs regulate the mitochondrial permeability transition pore through a common site.
PubMed:A ubiquinone-binding site regulates the mitochondrial permeability transition pore.
PubMed:Partial Purification and Characterization of Complex I, NADH:Ubiquinone Reductase, from the Inner Membrane of Beetroot Mitochondria.
PubMed:Ubiquinone-5 is reduced by superoxide in the aerobic state by NADPH oxidase of guinea pig macrophages.
PubMed:The inhibition of plant mitochondrial respiration by the synthetic analog of ubiquinone, 5-n-undecyl-6-hydroxy-4,7-dioxobenzothiazole (UHDBT).
PubMed:Characterization of purified cytochrome b-c1 complex from Rhodopseudomonas sphaeroides R-26.
PubMed:On the role of ubiquinone in the respiratory chain.
PubMed:Partial purification and properties of respiratory chain-linked l-glycerol 3-phosphate dehydrogenase from a marine bacterium, Vibrio alginolyticus.
PubMed:Inhibition of electron transfer in the cytochrome b-c, segment of the mitochondrial respiratory chain by a synthetic analogue of ubiquinone.
PubMed:Bioenergetics in clinical medicine: prevention by forms of coenzyme Q of the inhibition by adriamycin of coenzyme Q10-enzymes in mitochondria of the myocardium.
PubMed:Effect of alpha-p-chlorophenoxyisobutyrate on the metabolism of isoprenoid compounds in the rat.
PubMed:Isolation of ubiquinone-5, new member of ubiquinone group.
 
Notes:
None found
Please share your Comments.
Email Address:
Top of Page | Home
Copyright © 1980-2025 The Good Scents Company (tgsc) ™ | Disclaimer | Privacy Policy