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COENZYME Q1

Product Name
COENZYME Q1
CAS No.
727-81-1
Chemical Name
COENZYME Q1
Synonyms
Nsc 268269;COENZYME Q1;UBIQUINONE-5;Ubiquinone 1;Ubiquinone Q1;Coenzyme?Q1;Coenzyme Q1(solution in ethanol);2-Isopentenyl-5,6-dimethoxy-3-methyl-p-benzoquinone;2,3-DIMETHOXY-5-METHYL-6-(3-METHYL-2-BUTENYL)-1,4-BENZOQUINONE;2,3-dimethoxy-5-methyl-6-(3-methylbut-2-enyl)cyclohexa-2,5-diene-1,4-dione
CBNumber
CB8278506
Molecular Formula
C14H18O4
Formula Weight
250.29
MOL File
727-81-1.mol
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COENZYME Q1 Property

Boiling point:
389.1±42.0 °C(Predicted)
Density 
1.10±0.1 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
DMF: 10 mg/ml; Ethanol: 10 mg/ml
form 
Orange-red to red liquid.
color 
Orange to red
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Safety

Safety Statements 
23-24/25
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C7956
Product name
Coenzyme Q1
Purity
≥95%
Packaging
2mg
Price
$128
Updated
2025/07/31
Sigma-Aldrich
Product number
C7956
Product name
Coenzyme Q1
Purity
≥95%
Packaging
10mg
Price
$385
Updated
2025/07/31
Cayman Chemical
Product number
18741
Product name
Coenzyme Q1
Purity
≥98%
Packaging
1mg
Price
$49
Updated
2024/03/01
Cayman Chemical
Product number
18741
Product name
Coenzyme Q1
Purity
≥98%
Packaging
5mg
Price
$190
Updated
2024/03/01
Sigma-Aldrich
Product number
C7956
Product name
Coenzyme Q1
Purity
≥95%
Packaging
5x10mg
Price
$1550
Updated
2025/07/31
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COENZYME Q1 Chemical Properties,Usage,Production

Description

Cooenzyme Q10 (CoQ10) is a component of the electron transport chain and participates in aerobic cellular respiration, generating energy in the form of ATP. CoQ1 is an amphipathic CoQ10 homolog that has a tail consisting of five isoprene units. It has been used as an electron acceptor to study a range of oxidoreductases as isolated enzymes, in subcellular fractions, in intact cells in culture, and in perfused organs. Ubiquinone analogs, including CoQ1, impact mitochondrial permeability transition pore (PTP) formation, as well as PTP-dependent cell death, in an analog- and cell-specific manner.

Uses

Coenzyme Q1 has been used to measure the mitochondrial respiratory chain complex 1 activity.

Uses

Coenzyme Q1 is an electron acceptor and a component of the electron transport chain. It also play a role in the?mitochondrial permeability transition pore (PTP). Coenzyme Q1 is structurally similar to?coenzyme Q2 (C636450)?and?coenzyme Q10 (C636501).

Definition

ChEBI: Ubiquinones is any benzoquinone derived from 2,3-dimethoxy-5-methylbenzoquinone; one of a group of naturally occurring homologues. The redox-active quinoid moiety usually carries a polyprenoid side chain at position 6, the number of isoprenoid units in which is species-specific. Ubiquinones are involved in the control of mitochondrial electron transport, and are also potent anti-oxidants. It has a role as an Escherichia coli metabolite and a mouse metabolite. It is a prenylquinone and a member of 1,4-benzoquinones. It is functionally related to a 2,3-dihydroxy-5-methyl-1,4-benzoquinone.

General Description

Coenzyme Q (CoQ) is localized to the hydrophobic domain of the phospholipid bilayer of mitochondria, plasma lipoproteins, and other biological membranes. It is a ubiquinone homolog with a short isoprenoid side chain.

Biochem/physiol Actions

Coenzyme Q1 (CoQ1) is a 1 isoprenyl group (not naturally occurring) member of a family of ubiquinones that share a quinine chemical group but differ in the number of isoprenyl chemical subunits in their tail. The CoQ compounds are lipid soluble components of cell membranes where they perform multiple functions such as electron and proton transport. The most well studied CoQ compound is CoQ10. CoQ1 is frequently used in comparison studies on the effect of isoprenyl chain length on CoQ functions or distribution and to identify quinone reductases.

References

[1] ROMANA FATO. Steady-State Kinetics of the Reduction of Coenzyme Q Analogs by Complex I (NADH:Ubiquinone Oxidoreductase) in Bovine Heart Mitochondria and Submitochondrial Particles?[J]. Biochemistry Biochemistry, 1996, 35 8: 2705-2716. DOI: 10.1021/bi9516034
[2] FLAVIEN DEVUN. Ubiquinone analogs: a mitochondrial permeability transition pore-dependent pathway to selective cell death.[J]. PLoS ONE, 2010: e11792. DOI: 10.1371/journal.pone.0011792
[3] ROBERT D BONGARD. Coenzyme Q(1) as a probe for mitochondrial complex I activity in the intact perfused hyperoxia-exposed wild-type and Nqo1-null mouse lung.[J]. American journal of physiology. Lung cellular and molecular physiology, 2012: L949-58. DOI: 10.1152/ajplung.00251.2011

COENZYME Q1 Preparation Products And Raw materials

Raw materials

Preparation Products

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COENZYME Q1 Suppliers

Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51395
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80
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9803
Advantage
58
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60
Shenzhen Regent Biochemical Technology Co., Ltd.
Tel
0755-85201366 18938635012
Fax
0755-85201366
Email
sales@regentsciences.com
Country
China
ProdList
9751
Advantage
58
Rhawn Reagent
Tel
400-400-1332688 18019345275
Fax
400-133-2688
Email
amy@rhawn.cn
Country
China
ProdList
14948
Advantage
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Beijing OKA biological technology co., LTD
Tel
010-62971590 18548936886
Fax
010-62340519
Email
3462612863@qq.com
Country
China
ProdList
10063
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354; +17819995354
Email
marketing@targetmol.com
Country
United States
ProdList
32435
Advantage
58
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11218
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MedBioPharmaceutical Technology Inc
Tel
021-69568360 18916172912
Email
order@med-bio.cn
Country
China
ProdList
8140
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Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 15801484223;
Email
psaitong@jm-bio.com
Country
China
ProdList
29757
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58

727-81-1, COENZYME Q1Related Search:


  • 2,3-DIMETHOXY-5-METHYL-6-(3-METHYL-2-BUTENYL)-1,4-BENZOQUINONE
  • COENZYME Q1
  • UBIQUINONE-5
  • 2,3-dimethoxy-5-methyl-6-(3-methylbut-2-enyl)cyclohexa-2,5-diene-1,4-dione
  • Ubiquinone Q1
  • 2,3-Dimethoxy-5-methyl-6-(3-methyl-2-butenyl)-1,4-benzoquinone, Ubiquinone-1, Ubiquinone-5
  • 2,3-Dimethoxy-5-methyl-6-(3-methyl-2-butenyl)-2,5-cyclohexadiene-1,4-dione
  • 2-Isopentenyl-5,6-dimethoxy-3-methyl-p-benzoquinone
  • Ubiquinone 1
  • 2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3-methyl-2-butenyl)-
  • Nsc 268269
  • 2,5-Cyclohexadiene-1,4-dione, 2,3-dimethoxy-5-methyl-6-(3-methyl-2-buten-1-yl)-
  • Coenzyme?Q<sub>1</sub>
  • 2,3-Dimethoxy-5-methyl-6-(3-methylbut-2-en-1-yl)cyclohexa-2,5-diene-1,4-dione
  • Coenzyme Q1(solution in ethanol)
  • 727-81-1
  • Electron Transport and Cellular Respiration
  • Cofactors and Substrates
  • Metabolomics
  • Metabolic Pathways
  • BioChemical