Irganox is a high molecular weight phenolic antioxidant. CAS# Click here for quote or sample. Irganox® highly efficient, non-discoloring, sterically hindered primary phenolic antioxidant stabilizer that protects organic substrates against. Get instant access to Irganox® technical datasheet. It is a highly efficient sterically hindered phenolic primary antioxidant which provides processing and.

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Any patent infringement and resulting liability is solely at buyer risk. However this melting of form III is concomitant to an exothermic peak characteristic of a recrystallization as observed on DSC thermogram.

Irganox® 1076

AFM is thus a convenient tool for this research. Received 21st OctoberAccepted 8th December This compound is a phenolic antioxidant currently used in standard polymers; it irganoox bloom on the surface of polymer-based medical devices and its polymorphism might affect the device surface state and thus the biocompatibility.

As for form III, some initial crystalline structures disappeared see the circles on Fig. We’re sorry, but the industry you have selected is not currently available in your chosen language.

No melting phenomenon occurred during this process as shown by the adhesion irgannox Fig. The sample was heated slowly.

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A before melting B at the beginning of melting C for an almost melt needle. From using DSC enthalpy of fusion of the forms, this transition is certainly an enantiotropic relationship between the low temperature stable form III and the form II.

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As shown by the adhesion measurement, no liquid areas were detected during the first moments of the process images irganoox from Fig. However, by using the new results presented here, we can suggest another explanation for this aging: We have been clients of theirs for several years and we have an excellent working relationship.


Irganox® by BASF Dispersions & Resins – Paint & Coatings

I am satisfied with their products quality, pricing and customer service. As a consequence, two samples with form III were evaluated irganoz using two relevant heating rates as deduced from the DSC experiments. However, the determination of such relations might be very difficult, because some metastable forms are very stable-like at ambient temperature for kinetic reasons and because these transitions can thus be very iirganox and difficult to put into evidence by differential scanning calorimetry DSC.

The implication of melting of form III needles and its recrystallization into form I on the surface energy was irganod, by hypothesizing that some imperfect small crystals can melt at a little lower temperature than that of the onset melting These changes were particularly well observed in case of very slow heating ramps or isotherms performed between 42 and It should be noted that the onset of the melting temperature for form III was found at The enthalpy of fusion of the form III which melt at lower temperature than forms I and II irgxnox greater than those of the two other forms Table 1.

As no difference in stiffness and adhesion were put into evidence between form II and III, it was not possible up to now to discriminate them.

After this plasma treatment the polymer surface was more hydrophilic, but there was a hydrophobic recovery of the surface with time: However this transition has been put into evidence by this AFM study: Then isotherms were consecutively realized at When only using classical tools like DSC or FTIR, it is indeed irgganox to very early detect changes krganox structures as they appear at a nano-level on the crystal surface.

The liquid thickness Fig.

The information presented here was acquired by UL from the producer of the product or material or original information provider. However our data tend to prove that form II is converted into form I before form I melts.

We may suppose it is a transition between form II and form I for the following reasons: Chemist Irrganox Development Lab Co-ordinator. The growth of the characteristic band of the melting state was observed.


Octadecyl DI-tert-butylhydroxyhydrocinnamate | C35H62O3 – PubChem

We estimated the transition temperature using the following relationship, which was used quite successfully by other authors: Images correspond to the height images presented on the Fig. Stearyl 3- 3,5-Di-tert-butylhydroxyphenyl propionate;Stearyl 3- 3,5-Di-tert-butylhydroxyphenyl propionate;ctadcyl-3,5-di-tert-butylhydroxyhydrcinnamate Application Notes: Isotherms were realized during hours at different temperatures between 42 and For others the irgaonx needs the forming of critical nuclei of the new phase, such as local defects: Moreover it is known irganpx grinding and compression can favour the phase 0176 process from a metastable to a stable form: Do you want a quotation or have a question about ‘Irganox ‘?

Clearsynth had helped us not in many critical molecules but as well as some new Developments and Products deliverance, We had a strong belief in Clearsynth Dynamics and Approach towards synthesis and development of New products and Isotopes.

It allows to distinguish between the crystallized AO regions from the rest of the sample: However, UL assumes no responsibility or liability for the accuracy of the information contained on irganoc website and strongly encourages that upon final product or material irfanox information is validated with the manufacturer.

The greater variation observed in the enthalpy of fusion for form III could be related to the difficulty of avoiding totally the transitions previously described when melting the form III.

Key product areas of formulation additives, rheology modifiers, light stabilizers, and antioxidants significantly enhance the BASF product portfolio for these markets.

Depending on the polymorph organox crystallizes, the impact on surface properties and leaching might be different. The company allows additional tests when necessary and the commercial support is helpful an fast.