80387-98-0 Usage
Chemical structure
A complex compound with multiple functional groups, including amine and piperidinyl groups.
Molecular weight
High molecular weight.
Functionality
Triazine-based stabilizer.
Application
Used in polymers and plastics to protect them from the degrading effects of light and heat.
Antioxidant properties
The presence of amine and piperidinyl groups contribute to its antioxidant properties.
UV-stabilizing properties
The compound is effective in extending the lifespan and maintaining the appearance of polymer materials.
Industrial applications
Valuable in various industrial applications due to its ability to protect polymers and plastics from degradation.
Appearance
The compound is likely a solid or a viscous liquid, although the exact appearance is not specified in the material provided.
Solubility
The solubility of the compound is not specified in the material provided, but it is likely soluble in organic solvents due to its nonpolar nature.
It is important to note that the specific content and properties of this chemical may vary depending on the specific formulation and application. Additionally, the material provided does not include information on the toxicity, environmental impact, or regulatory status of this compound, which may also be important considerations in its use and handling.
Check Digit Verification of cas no
The CAS Registry Mumber 80387-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,8 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80387-98:
(7*8)+(6*0)+(5*3)+(4*8)+(3*7)+(2*9)+(1*8)=150
150 % 10 = 0
So 80387-98-0 is a valid CAS Registry Number.
80387-98-0Relevant articles and documents
Preparation method of hindered amine light stabilizer
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Paragraph 0048; 0049; 0051; 0052; 0054; 0055, (2020/04/06)
The invention relates to a preparation method of a hindered amine light stabilizer. The method comprises the following steps: reacting cyanuric chloride with N,N'-bis(3-aminopropyl)ethylenediamine toobtain an intermediate I; reacting the intermediate I with N-butyl-2,2,6,6-tetramethyl-4-piperidylamine to obtain an intermediate II; and adding paraformaldehyde or formaldehyde and formic acid, and carrying out a methylation reaction to obtain the target product. The method adopting the above new synthetic route has the advantages of avoiding of high-temperature or high-pressure reaction conditions in preparation, improvement of the density of hindered amine functional groups of the product, high purity, avoiding of the step of possibly generating hydrolysis byproducts, and great reduction ofthe industrial production cost of the product.