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Cytochrome P450
2,6-Dimethylquinoline - 98%, high purity , CAS No.877-43-0

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2,6-Dimethylquinoline - 98%, high purity , CAS No.877-43-0

COA

Grade & Purity:

≥98%

Cas Number: 877-43-0
Molecular Weight: 157.22
Beilstein Registry Number: 20408
MDL number: MFCD00006762
PubChem CID: 13414
PubChem SID: 504752450

In stock

Item Number

D136801

Grouped product items
SKU	Size	Availability	Price
D136801-1g	1g	3	$21.90
D136801-5g	5g	3	$98.90
D136801-25g	25g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$442.90
D136801-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,592.90

View related series

Cytochrome P450 (241) Lipid metabolism (1912) Metabolic Enzyme/Protease (4860) Pyridines (1259) Six-Membered Heterocyclic Compounds (1696)

Basic Description

Synonyms	Quinoline, 2,6-dimethyl \| Quinoline, 2,6-dimethyl- \| AMY28857 \| Z56969311 \| D1236 \| p-Toluquinaldine \| EINECS 212-891-5 \| F17612 \| PD158272 \| 2.6-Dimethylquinoline \| FT-0633059 \| EU-0000308 \| SB67469 \| NSC-1782 \| AS-48061 \| SY016998 \| DTXSID0044153 \| SCHE
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	2,6-Dimethylquinoline is the chemical constituent present in roots of Peucedantu praeruptorum. It is a potential inhibitor of cytochrome P450 1A2 activity.
Storage Temp	Argon charged
Shipped In	Normal
Product Description	2,6-Dimethylquinoline was used to study the inhibition potencies (IC50 values) of structurally diverse chemicals with recombinant human CYP2B6 enzyme for in vitro research purposes.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Quinolines and derivatives

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Quinolines and derivatives
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Quinolines and derivatives
Alternative Parents	Methylpyridines Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Quinoline - Methylpyridine - Benzenoid - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as quinolines and derivatives. These are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

Discover Target: CYP1A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2A6 Tchem Cytochrome P450 2A6 (2861 Activities)

Discover Target: CYP2A6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Cyp2a5 Cytochrome P450 2A5 (126 Activities)

Discover Target: Cyp2a5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504752450
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504752450
IUPAC Name	2,6-dimethylquinoline
INCHI	InChI=1S/C11H11N/c1-8-3-6-11-10(7-8)5-4-9(2)12-11/h3-7H,1-2H3
InChIKey	JJPSZKIOGBRMHK-UHFFFAOYSA-N
Smiles	CC1=CC2=C(C=C1)N=C(C=C2)C
Isomeric SMILES	CC1=CC2=C(C=C1)N=C(C=C2)C
WGK Germany	3
Molecular Weight	157.22
Beilstein	20408
Reaxy-Rn	2545
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2545&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot Number	Certificate Type	Date	Item
F2325437	Certificate of Analysis	Apr 09, 2025	D136801
F2325395	Certificate of Analysis	Apr 09, 2025	D136801
C2214364	Certificate of Analysis	Dec 12, 2023	D136801
C2214110	Certificate of Analysis	Dec 12, 2023	D136801
C2214154	Certificate of Analysis	Dec 12, 2023	D136801
C2214155	Certificate of Analysis	Dec 12, 2023	D136801
C1516177	Certificate of Analysis	Sep 13, 2022	D136801

Chemical and Physical Properties

Sensitivity	Air Sensitive
Boil Point(°C)	267 °C
Melt Point(°C)	58 °C
Molecular Weight	157.210 g/mol
XLogP3	3.000
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	157.089 Da
Monoisotopic Mass	157.089 Da
Topological Polar Surface Area	12.900 Å²
Heavy Atom Count	12
Formal Charge	0
Complexity	155.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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