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2-Benzotriazol-2-yl-4-tert-butyl-6-methyl-phenol, commonly known as UV-327 or Tinuvin 327, is a widely used UV stabilizer and light stabilizer in the chemical industry. 2-benzotriazol-2-yl-4-tert-butyl-6-methyl-phenol belongs to the class of hindered amine light stabilizers (HALS) and is effective in protecting materials from the harmful effects of ultraviolet (UV) radiation. It is particularly useful in the stabilization of polymers, such as plastics and coatings, against photodegradation, which can lead to discoloration, embrittlement, and loss of mechanical properties. UV-327 is known for its high efficiency, low volatility, and excellent compatibility with various substrates, making it a popular choice for applications in the automotive, construction, and packaging industries.

4860-07-5

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4860-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4860-07-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,6 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4860-07:
(6*4)+(5*8)+(4*6)+(3*0)+(2*0)+(1*7)=95
95 % 10 = 5
So 4860-07-5 is a valid CAS Registry Number.

4860-07-5Upstream product

4860-07-5Downstream Products

4860-07-5Relevant academic research and scientific papers

Preparation of Some 2-(2' H-Benzotriazol-2'-yl)phenol Ultraviolet Absorbers: Application of the Transalkylation Reaction

Rosevear, Judi,Wilshire, John F.K.

, p. 1163 - 1176 (2007/10/02)

When 2-(2' H-benzotriazol-2'-yl)phenols containing t-alkyl substituents are warmed in toluene solution with an aluminium chloride/nitromethane catalyst, the t-alkyl groups are transferred to the solvent (toluene).This transalkylation reaction has been used to prepare not readily accessible or previously inaccessible 2-(2' H-benzotriazol-2'-yl)phenols, a class of ultraviolet absorbers widely used in industry.

Process for the production of 2-aryl-2H-benzotriazoles

-

, (2008/06/13)

An improved process for the production of 2-aryl-2H-benzotriazoles by the reduction of o-nitroazobenzene intermediates with zinc in alkaline medium comprises employing a ratio of moles of alkali to moles of o-nitroazobenzene intermediate in the range of 0.2-1.7/1 in the presence of less than 150 ppm of iron based on zinc used. The improved process results in higher yields of high purity products with a concomitant reduction in the amount of undesired cleavage amine by-products and a reduction in effluent pollution problems. The process is carried out in a polar/non-polar solvent mixture.

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