HEXAMOLL DINCH PDF

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1,2-Cyclohexane dicarboxylic acid diisononyl ester is a plasticizer for the manufacture of Hexamoll® DINCH is listed in Annex I of Regulation (EU) No 10 / by as Food Conctact Material (FCM) by its chemical name, i.e. as 1. New Plasticizer Hexamoll DINCH. Presentation (PDF Available) · July with Reads. DOI: /RG Plasticizer, Brussels. Get instant access to Hexamoll® DINCH technical datasheet. This plasticizer is suitable for use in toys, medical devices, food packaging, sports equipment etc.

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Toxicity of Hexamoll(®) DINCH(®) following intravenous administration.

From Wikipedia, the free encyclopedia. Their research at a fertility clinic showed that women who had been exposed to DINCH had lower, but statistically not significant estradiol hormone levels and fewer, again not statistically significant number of oocytes in their ovaries.

Opinion of the Hesamoll Panel on food additives, flavourings, processing aids and materials in contact with food AFC on a request related to a 12th list of substances for food contact materialsEFSA-Journal,—, 1— This page was last edited on 16 Decemberat Keeping Up With Additives.

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Consumer Product Safety Commission “strongly encourages the appropriate U. Journal of Exposure Science and Environmental Epidemiology.

A US federal law was passed in banning the use of some phthalates in children’s toys. Views Read Edit View history.

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From a chemical point of view it belongs to the group of aliphatic esters. In the European Union the European Food Safety Authority has approved 1,2-cyclohexane dicarboxylic acid diisononyl ester for a wide variety of food contact applications in October By using this site, you agree to the Terms of Use and Privacy Policy.

It remains unclear why this Research Group was not able to identify the published human biomonitoring data which give a perfect overview on population exposure of alternative plasticizers e. However, urinary MHiNCH concentrations were unrelated to mature oocyte yield and endometrial wall thickness.

Toxicity of Hexamoll(®) DINCH(®) following intravenous administration.

The two commercial routes to manufacture 1,2-cyclohexane dicarboxylic acid diisononyl ester are the catalytic hexaomll of diisononyl phthalate [4] [5] and the Diels-Alder reaction of a maleic acid ester with 1,3-butadiene followed hexamlll hydrogenation. In the case of the catalytic hydrogenation the aromatic, planar part of the diisononyl phthalate is transformed to a cyclohexane ring by a formal addition of 6 hydrogen atoms while the alkyl and ester groups are not affected by the hydrogenation.

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Federal ban on a chemical used in toys will affect Texas. Science of the Total Environment. Not classified as a dangerous substance [2].

Retrieved from ” https: A French group from the University of Clermont-Ferrand noted that clinical data and data regarding the migration from Medical Devices would be rare.