This MedLibrary.org supplementary page on 4-Methylbenzylidene camphor is provided directly from the open source Wikipedia as a service to our readers. Please see the note below on authorship of this content, as well as the Wikipedia usage guidelines. To search for other content from our encyclopedia supplement, please use the form below:
Related Sponsors
| 4-Methylbenzylidene camphor1 | |
|---|---|
 |
|
| IUPAC name | (3E)-1,7,7-Trimethyl-3-[(4-methylphenyl)methylene]-2-norbornanone |
| Other names | 3-(4-Methylbenzylidene)bornan-2-one 3-(4-Methylbenzylidene)-dl-camphor |
| Identifiers | |
| Abbreviations | 4-MBC |
| CAS number | 36861-47-9 |
| PubChem | |
| EINECS number | |
| SMILES |
|
| Properties | |
| Molecular formula | C18H22O |
| Molar mass | 254.37 g/mol |
| Appearance | White crystalline powder |
| Melting point |
66-69 °C |
| Solubility in water | Insoluble |
| Hazards | |
| Main hazards | Xi |
| R-phrases | R36/37/38 R50 R53 |
| S-phrases | S26 S37/39 S61 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references |
|
4-Methylbenzylidene camphor (4-MBC) is an organic camphor derivative that is used in the cosmetic industry for its ability to protect the skin against UV, specifically UV B radiation. As such it is used in sunscreen lotions and deodorants. Its tradenames include Eusolex 6300 (Merck) and Parsol 5000 (DSM).
Contents |
Mechanism
All the camphor sunscreens are supposed to dissipate the photon energy by cis-trans isomerisation. But for 4-MBC the quantum yield for this isomerisation is reported to be only between 0.13 - 0.3. This low quantum yield means that other photochemical processes are occurring.2
Endocrine disruptor
Studies have raised the issue that 4-MBC acts an endocrine disruptor. There is controversy about the estrogenic effects of 4-MBC and while one study showed only a relatively minor effect,3 a study in Switzerland showed significant uterine growth in immature rodents.4 In addition, there is some evidence that 4-MBC may suppress the pituitary-thyroid axis leading to hypothyroidism.5
The agent can also lead to a photoallergic dermatitis.citation needed
Approval status
4-MBC is approved for use in Europe by the European Union's Scientific Committee for Cosmetic Products & Non-Food Products and it is approved in Canada by Health Canada. It is not approved for use in the USA by the Food and Drug Administration and it is not permitted in Japan.
See also
References
- ^ 3-(4-METHYLBENZYLIDEN)CAMPHOR at chemicalland21.com
- ^ Sun Protection in Man. Chapter 26: Cantrell, Ann; McGarvey, David J.; Truscott, T. George. Photochemical and photophysical properties of sunscreens.
- ^ Mueller SO, Kling M, Arifin Firzani P, et al (April 2003). "Activation of estrogen receptor alpha and ERbeta by 4-methylbenzylidene-camphor in human and rat cells: comparison with phyto- and xenoestrogens". Toxicol. Lett. 142 (1-2): 89–101. PMID 12765243. http://linkinghub.elsevier.com/retrieve/pii/S037842740300016X.
- ^ Sun Block has Endocrine Disruptor Chemicals, New Scientist, April 18, 2001
- ^ IH Hamann, C Schmutzler, P Kirschmeyer, H Jarry & J Köhrle (2006). "4-Methylbenzylidene-camphor (4MBC) causes pituitary effects comparable to hypothyroidism". Endocrine Abstracts 11: OC60. http://www.endocrine-abstracts.org/ea/0011/ea0011oc60.htm.
|
|||||||||||||||||
Wikipedia content modification information:
- This page was last modified on 3 January 2009, at 16:09.
Wikipedia Authorship and Review
Wikipedia content provided here is not reviewed directly by MedLibrary.org. Wikipedia content is authored by an open community of volunteers and is not produced by or in any way affiliated with MedLibrary.org.
Wikipedia Usage Guidelines
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article on "4-Methylbenzylidene camphor".
The URL for this specific entry is:
All Wikipedia text is available under the terms of the GNU Free Documentation License. (See Copyrights for details). Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc.