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  • 116244-12-3 Structure
  • Basic information

    1. Product Name: Uvinul T 150
    2. Synonyms:
    3. CAS NO:116244-12-3
    4. Molecular Formula: C48H66N6O6
    5. Molecular Weight: 823.07424
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116244-12-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Uvinul T 150(CAS DataBase Reference)
    10. NIST Chemistry Reference: Uvinul T 150(116244-12-3)
    11. EPA Substance Registry System: Uvinul T 150(116244-12-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 116244-12-3(Hazardous Substances Data)

116244-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116244-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,4 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116244-12:
(8*1)+(7*1)+(6*6)+(5*2)+(4*4)+(3*4)+(2*1)+(1*2)=93
93 % 10 = 3
So 116244-12-3 is a valid CAS Registry Number.

116244-12-3Downstream Products

116244-12-3Relevant articles and documents

Preparation method of sun-screening agent octyl triazinone

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Paragraph 0091; 0095; 0098-0112, (2021/02/06)

The invention discloses a preparation method of a sun-screening agent octyl triazinone, octyl triazinone prepared by the preparation method and an application of octyl triazinone, and the method comprises the following steps: step 1, carrying out esterification reaction on p-nitrobenzoic acid and isooctyl alcohol to obtain a product I, 2, carrying out a hydrogenation reaction on the product I in the presence of a catalyst, filtering after the reaction is completed, and carrying out reduced pressure distillation to obtain a product II, and step 3, adding a solvent into the product II, heating to reflux, adding the solution A, carrying out a reaction, and carrying out post-treatment to obtain octyltriazinone. Cheap and easily available p-nitrobenzoic acid is used as a raw material, the sun-screening agent octyl triazinone is efficiently prepared through esterification, hydrogenation and coupling, meanwhile, iso-octyl p-aminobenzoate is obtained, the obtained octyl triazinone is high in chromatographic purity and yield, and the method has the advantages of being few in three wastes, low in cost, green, environmentally friendly, easy to operate, easy to control and the like.Easy realization of industrial production.

An ultraviolet absorbent octyl triazone synthetic method

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, (2017/08/26)

The invention relates to a synthetic method for an ultraviolet absorbent--octyl triazone. The method comprises the following steps: with sodium bisulfate as a catalyst, reacting p-nitrobenzoic acid with isooctanol under the action of toluene so as to prep

Method for preparing ultraviolet light absorber UVT-150

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Paragraph 0017; 0019; 0021, (2017/08/31)

The invention discloses a method for preparing an ultraviolet light absorber UVT-150. The method is composed of the following process steps: (1) carrying out an aryl amination reaction, namely adding methyl p-aminobenzoate and an organic solvent into a re

Crystalline form of a triazine derivative, the procedure for its production and cosmetic formulations thereof

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Paragraph 0063-0064, (2014/09/29)

Disclosed is a crystalline form of the compound of formula (I), characterised by an endothermic melting transition between 20 and 30 J/g at temperatures from 125°C to 135°C, determined by differential scanning calorimetry (DSC) and by its X-ray diffractio

CRYSTALLINE FORM OF A TRIAZINE DERIVATIVE AND THE PROCEDURE FOR ITS PRODUCTION

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Paragraph 0095-0096, (2014/09/29)

Disclosed is a crystalline form of the compound of formula (I), characterised by an endothermic melting transition between 20 and 30 J/g at temperatures from 125° C. to 135° C., determined by differential scanning calorimetry (DSC) and by its X-ray diffraction spectrum.

TRIAZINE DERIVATIVES

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Paragraph 0100; 0101; 0102; 0103; 0104, (2013/11/05)

The invention relates to novel intermediates for the preparation of substituted triazines used in particular in the cosmetic, detergent, coating, plastics and textile industries. The invention also relates to the processes for preparation of said intermed

TRIAZINE DERIVATIVES

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Page/Page column 22; 23, (2013/11/05)

The invention relates to novel intermediates for the preparation of substituted triazines used in particular in the cosmetic, detergent, coating, plastics and textile industries. The invention also relates to the processes for preparation of said intermed

COSMETIC COMPOSITIONS COMPRISING AN ESTER DERIVED FROM 4-CARBOXY-2-PYRROLIDINONE AND A LIPOPHILIC SCREENING AGENT; USE OF SAID DERIVATIVE AS A SOLVENT FOR A BENZOPHENONE LIPOPHILIC SCREENING AGENT

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, (2012/11/07)

The present invention relates to a composition comprising, in a cosmetically acceptable medium, at least one ester derived from 4-carboxy-2-pyrrolidinone, of formula (I) below: in which: R1 denotes a linear or branched C1-C20 alkyl radical,R2 denotes a linear or branched C1-C20 alkyl radical that may contain a C5-C6 ring, the phenyl radical, the benzyl radical or the phenethyl radical,and at least one benzophenone-type lipophilic UV screening agent. The present invention also relates to the use of at least one ester derived from 4-carboxy-2-pyrrolidinone, of formula (I), as defined above, in a composition comprising, in a cosmetically acceptable medium, at least one benzophenone-type lipophilic UV screening agent, as a solvent for said benzophenone screening agent, in and/or as an agent for improving the solubility of said benzophenone screening agent in said composition or with the aim of improving the sun protection factor.

COSMETIC TREATMENT METHOD USING A COMPOUND THAT CAN BE CONDENSED IN SITU AND A UV-RADIATION-FILTERING AGENT

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, (2013/02/28)

The present invention relates to a method for the cosmetic treatment of the skin, comprising the application, to the skin: of a compound or group of compounds A capable of condensing in situ and exhibiting at least one reactive functional group FA which is free after condensation; and of a screening agent C which screens out UV radiation, comprising a reactive functional group FC capable of forming a covalent bond or a physical (ionic, hydrogen) bond by reaction with the functional group FA.

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