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31301-28-7

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31301-28-7 Usage

Description

4-Methyl-1,10-phenanthroline (4-Mephen) is a methyl-substituted phenanthroline, a type of heterocyclic compound with a tricyclic structure. It is commonly used as a ligand in various chemical and analytical applications due to its ability to form stable complexes with metal ions.

Uses

Used in Chemical Synthesis:
4-Methyl-1,10-phenanthroline is used as a starting material for the production of 1,10-Phenanthrolin-4-aldehyde, which is an important intermediate in the synthesis of various organic compounds and pharmaceuticals.
Used in Analytical Chemistry:
As a ligand, 4-methyl-1,10-phenanthroline is employed in analytical chemistry for the detection and determination of metal ions, particularly those of iron and cobalt. It forms colored complexes with these metal ions, which can be used for their quantitative analysis.
Used in Coordination Chemistry:
In coordination chemistry, 4-methyl-1,10-phenanthroline is used as a bidentate ligand to form complexes with various metal ions. These complexes have applications in areas such as catalysis, molecular magnetism, and the development of new materials with unique properties.
Used in Pharmaceutical Industry:
The complexes formed by 4-methyl-1,10-phenanthroline with certain metal ions have potential applications in the pharmaceutical industry, as they may exhibit biological activities such as anti-cancer, anti-inflammatory, or anti-microbial properties.
Used in Environmental Applications:
4-Methyl-1,10-phenanthroline and its metal complexes can also be utilized in environmental applications, such as the removal of heavy metal ions from contaminated water or soil, due to their high affinity for these ions.

Check Digit Verification of cas no

The CAS Registry Mumber 31301-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,0 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 31301-28:
(7*3)+(6*1)+(5*3)+(4*0)+(3*1)+(2*2)+(1*8)=57
57 % 10 = 7
So 31301-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2/c1-9-6-8-15-13-11(9)5-4-10-3-2-7-14-12(10)13/h2-8H,1H3

31301-28-7 Well-known Company Product Price

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  • Alfa Aesar

  • (31888)  4-Methyl-1,10-phenanthroline   

  • 31301-28-7

  • 1g

  • 617.0CNY

  • Detail
  • Alfa Aesar

  • (31888)  4-Methyl-1,10-phenanthroline   

  • 31301-28-7

  • 5g

  • 2482.0CNY

  • Detail

31301-28-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-METHYL-1,10-PHENANTHROLINE

1.2 Other means of identification

Product number -
Other names 4-methyl-phen

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:31301-28-7 SDS

31301-28-7Relevant articles and documents

OXIDATION-REDUCTION MECHANISMS - INNER-SPHERE AND OUTER-SPHERE ELECTRON TRANSFER IN THE REDUCTION OF IRON(III), RUTHENIUM(III), AND OSMIUM(III) COMPLEXES BY ALKYL RADICALS. MECHANISMS -

Rollick,Kochi

, p. 1319 - 1330 (2007/10/02)

Alkyl radicals are readily oxidized by the tris(phenanthroline) and tris(bipyridine) complexes ML//3**3** plus of iron(III), ruthenium(III), and osmium(III) in acetonitrile solution, the second-order rate constants easily exceeding 10**6 M** minus **1s** minus **1 at 25 degree C. Two oxidative processes are identified as (a) ligand substitution on the coordinated 1,10-phenanthroline to yield various alkylphenanthrolines and (b) cation formation to afford alkenes and N-alkylacetamides (after hydrolysis). Cation formation is characterized by extensive skeletal rearrangement of neopentyl, isobutyl, and n-propyl groups, whereas ligand substitution by the same alkyl radicals occurs without any rearrangement.

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