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1-Methyl-2-undecyl-1,4-dihydroquinoline-4-one, commonly known as Uviton 132, is a chemical compound that functions as a UV absorber and light stabilizer. It is characterized by its capacity to absorb ultraviolet light and convert it into low-energy heat, thereby preventing the degradation of materials it is incorporated into.

59443-02-6

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59443-02-6 Usage

Uses

Used in Plastics Industry:
1-Methyl-2-undecyl-1,4-dihydroquinoline-4-one is used as a UV stabilizer and absorber for plastics to protect them from UV-induced degradation, ensuring their durability and longevity when exposed to sunlight.
Used in Rubber Industry:
In the rubber industry, 1-Methyl-2-undecyl-1,4-dihydroquinoline-4-one serves as a light stabilizer, enhancing the resistance of rubber products to UV radiation, which can cause discoloration and physical property degradation.
Used in Adhesives:
1-Methyl-2-undecyl-1,4-dihydroquinoline-4-one is used as a UV absorber in adhesives to maintain their bonding strength and integrity when exposed to sunlight, preventing the deterioration that can occur due to UV exposure.
Used in Coatings:
1-Methyl-2-undecyl-1,4-dihydroquinoline-4-one is utilized as a light stabilizer in coatings to shield the underlying materials from the harmful effects of UV radiation, preserving the color and structural integrity of coated surfaces.
Used in Personal Care Products:
In the personal care sector, 1-Methyl-2-undecyl-1,4-dihydroquinoline-4-one is used as an ingredient in sunscreens and other skincare products to enhance their UV protection capabilities, safeguarding the skin from the damaging effects of the sun's rays.

Check Digit Verification of cas no

The CAS Registry Mumber 59443-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,4 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59443-02:
(7*5)+(6*9)+(5*4)+(4*4)+(3*3)+(2*0)+(1*2)=136
136 % 10 = 6
So 59443-02-6 is a valid CAS Registry Number.

59443-02-6SDS

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 1-methyl-2-undecylquinolin-4-one

1.2 Other means of identification

Product number -
Other names 1-methyl-2-undecyl-1H-quinolin-4-one

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:59443-02-6 SDS

59443-02-6Downstream Products

59443-02-6Relevant academic research and scientific papers

Quinolone alkaloids from Evodia rutaecarpa

Tang, Yuan-Qing,Feng, Xiao-Zhang,Huang, Liang

, p. 719 - 722 (2007/10/03)

Five new quinolone alkaloids were isolated from the fruits of Evodia rutaecarpa, together with seven known ones. Their structures were determined on the basis of spectral data and chemical reactions.

The Chemistry of 2H-3,1-Benzoxazine-2,4(1H)-dione (Isatoic Anhydride). 17. Synthesis of 2-Alkyl-4-quinolone Alkaloids via a One-step Reaction of N-Methylisatoic Anhydride with Methyl Ketone Enolates

Coppola, Gary M.

, p. 491 - 494 (2007/10/02)

Lithium enolates derived from aliphatic methyl ketones react with N-methylisatoic anhydride (5) at -78 deg C to give 2-alkyl-4-quinolone alkaloids 7 in a single step.The method was used to synthesize both double bond isomers of 1-methyl-2-(8-tridecenyl)-4(1H)-quinolinone (8) thereby showing that the alkaloid evocarpine possesses the Z-olefin stereochemistry 8a.Reduction of 8a provided the alkaloid dihydroevocarpine (16).Compound 16 was also directly prepared from the reaction of 5 with the lithium enolate of 2-pentadecanone.

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