5581-32-8Relevant articles and documents
Interaction of a Vinylic Organosol Used as Can Coating with Solvents and Food Simulants
Cottier,Feigenbaum,Mortreuil,Reynier,Dole,Riquet
, p. 5254 - 5261 (1998)
Metal cans are often protected from corrosion by vinylic organosol coatings, made from PVC and epoxyphenolic (EP) resins. Using electron spin resonance, BADGE, a monomer of EP, was shown to plasticize PVC. Optimization of extraction allowed extraction of 4 mg of BADGE/dm2, so vinylic organosols appear to be worst-case coatings. Comparison of behavior between BADGE and a paramagnetic probe revealed that these compounds were trapped to a large extent in the cross-linked EP network and could not migrate at 40 °C. Contact with triglycerides, which plasticize the coating, induced high migration of BADGE. Neither isooctane nor ethanol could mimic fats, in contrast to isooctane/tert-butyl acetate mixtures. In aqueous foodstuffs, BADGE hydrolyzed into a monoepoxide and then into a bisdiol. The total amount of toxicologically relevant epoxides over shelf life was shown to reach a maximum value within 3 weeks at 40 °C, at very low levels, whatever the aqueous food simulant. After sterilization at 120 °C (20 min), the level of BADGE in the migrate is very low, whereas up to 2 mg of hydrolysis products is found in the liquid/dm2. During further storage at 40 °C, the amount of epoxides rapidly decreases.
A PROPYL-PHENYL-ETHER DERIVATIVE, AND MELANOGENESIS INHIBITOR, SKIN-LIGHTENING AGENT, ANTIMICROBIAL AGENT AND COSMETIC CONTAINING SAID PROPYL-PHENYL-ETHER DERIVATIVE
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Paragraph 0316-0319, (2016/12/12)
Provided is a compound that exhibits an excellent melanogenesis-inhibiting effect (skin-lightening effect), exhibits an excellent antimicrobial effect, excels in terms of temporal stability and the like, and is suitable for use as an ingredient of a cosmetic. Said compound is a propyl-phenyl-ether derivative compound comprising a propyl group that has a substituent such as a hydroxyl group and is bound to the hydroxyl group of a phenol group that has a substituent such as a tert-butyl group. A melanogenesis inhibitor, skin-lightening agent, and antimicrobial agent containing the aforementioned compound as an active ingredient are also provided, as is a cosmetic characterized by containing said compound.
Dermal penetration and metabolism of five glycidyl ethers in human, rat and mouse skin
Boogaard,Denneman,Van Sittert
, p. 469 - 483 (2007/10/03)
1. Glycidyl ethers (GE), an important class of industrial chemicals, are considered to be potentially mutagenic in vivo because some GE have been shown to be direct mutagens in short-term in vitro tests. 2. The percutaneous penetration and metabolism of representatives of different classes of GE was studied in the fresh, full-thickness C3H mouse, and dermatomed human and Fisher 344 rat skin to determine th apparent permeability constants, lag times and metabolic profiles. 3. Five different GE, the diglycidyl ethers of bisphenol A (BADGE), 4,4'-dihydroxy-3,3',5,5'-tetramethylbiphenyl (Epikote YX4000) and 1,6-hexanediol (HDDGE) and the GE of 1-dodecanol (C12GE) and o-cresol (o-CGE), were synthesized by reaction of their alcohols with epichlorohydrin. Their radiolabelled analogues were synthesized with a 14C-label using [U-14C]-epichlorohydrin. 4. There was a large variation (four orders of magnitude) in percutaneous penetration between the five GE. In general, penetration through full-thickness mouse skin was higher than through dermatomed rat skin, whereas dermatomed human skin was the least permeable. The permeability increased in the order YX4000 12GE 12GE and o-CGE penetrated the skin unchanged. For o-CGE, but none of the other GE, the percentage of the applied dose that penetrated the skin unchanged increased over time. 7. The large variation in response observed with the five selected GE indicates that GE should not be considered as a single class of compounds but rather on the basis of their individual properties.
