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OverviewThe Deceth ingredients (Deceth-3, Deceth-4, Deceth-5, Deceth-6, Deceth-7, Deceth-8, Deceth-9, Deceth-10) are polyethylene glycol ethers of decyl alcohol. The number in the name indicates the average number of units of ethylene oxide in the molecule. Sims 4 mod teenage romance with adults. In cosmetic and personal care products, the Deceth ingredients are primarily used in the formulation of hair dyes and colors and other hair care products.
All of the Deceth ingredients function as surfactant -- emulsifying agents.
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The Deceth ingredients are produced by reacting ethylene oxide with decyl alcohol. The numerical designation refers to the average number of repeating ethylene oxide units in the molecule. Decyl alcohol is a fatty alcohol with 10 carbon atoms. The fatty alcohols in the other polyethylene glycol ether compounds reviewed by CIR include lauryl alcohol with 12 carbons, stearyl alcohol with 18 carbons, and cetearyl alcohol which is a mixture of cetyl alcohol (16 carbons) and stearyl alcohol.
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SafetyThe safety of the Deceth ingredients has been assessed by the Cosmetic Ingredient Review (CIR) Expert Panel as part of the review of the alkyl PEG ethers group of ingredients. The CIR Expert Panel evaluated the scientific data and concluded that the alkyl PEG ethers, including the Deceth ingredients were safe as used in cosmetic products when formulated to be non-irritating.
CIR Review:
Based on similar structures, the CIR Expert Panel determined that the alkyl PEG ether compounds, including the Deceth ingredients could be reviewed together. Developmental and reproductive toxicity studies as well as mutagenicity data were all negative for these compounds. These compounds can irritate the skin. Therefore, the CIR Expert Panel concluded that the Deceth ingredients, as well as the other alkyl PEG ether ingredients were safe as used when formulated to be nonirritating. Small amounts of 1,4-dioxane, a by-product of ethoxylation, may be found in the Deceth ingredients. The potential presence of this material is well known and can be controlled through purification steps to remove it from the ingredients before blending into cosmetic formulations.
More information about 1,4-dioxane.
A text 2 35 58. The Deceth ingredients may be used in cosmetics and personal care products marketed in Europe according to the general provisions of the Cosmetics Regulation of the European Union.
Power lines game. Link to the EU Cosmetic Regulation: http://europa.eu/legislation_summaries/consumers/product_labelling_and_packaging/co0013_en.htm
Deceth ingredients are polyethylene glycol ethers of Decyl alcohol that contain repeating ethylene oxide units. These ingredients are useful in cosmetics and personal care products as surfactant -- emulsifying agents.
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EU Cosmetics Inventory http://ec.europa.eu/consumers/cosmetics/cosing/
| Names | |
|---|---|
| IUPAC name 2-[(1R,6R)-3-Methyl-6-(1-methylethyl)-2-cyclohexen-1-yl]-5-pentyl-1,3-benzenediol | |
| Other names | |
| Identifiers | |
3D model (JSmol) | |
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| Properties | |
| C21H32O2 | |
| Molar mass | 316.485 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references |
8,9-Dihydrocannabidiol (H2CBD) is a synthetic cannabinoid that is closely related to cannabidiol (CBD) itself.[1] It was shown to have anti-seizure activity essentially identical to that of CBD in tests with rats. It may have certain advantages over CBD, in that it is fully synthetic, inexpensive to produce, and it is not a scheduled drug (cannabis extracts are controlled substances in most parts of the world). In addition, there is no path to synthesize the psychoactive substance tetrahydrocannabinol (THC) from H2CBD. CBD has been shown to convert to some extent to THC in the gastric tract,[2][3] and the deliberate laboratory conversion of CBD to THC is simple.[4][5] H2CBD has therefore been studied for its potential use as an alternative to CBD in terms of its lack of abuse liability and absence of psychotropic effects.[1]
References[edit]
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- ^ abMascal, M.; Hafezi, N.; Wang, D.; Hu, Y.; Serra, G.; Dallas, M. L.; Spencer, J. P. E. (2019). 'Synthetic, non-intoxicating 8,9-dihydrocannabidiol for the mitigation of seizures'. Scientific Reports. 9 (1): 7778. Bibcode:2019NatSR.9.7778M. doi:10.1038/s41598-019-44056-y. PMC6533278. PMID31123271.
- ^Merrick, John; Lane, Brian; Sebree, Terri; Yaksh, Tony; O'Neill, Carol; Banks, Stan L. (2016). 'Identification of Psychoactive Degradants of Cannabidiol in Simulated Gastric and Physiological Fluid'. Cannabis and Cannabinoid Research. 1 (1): 102–112. doi:10.1089/can.2015.0004. PMC5576596. PMID28861485.
- ^Watanabe, Kazuhito; Itokawa, Yuka; Yamaori, Satoshi; Funahashi, Tatsuya; Kimura, Toshiyuki; Kaji, Toshiyuki; Usami, Noriyuki; Yamamoto, Ikuo (2007). 'Conversion of cannabidiol to Δ9-tetrahydrocannabinol and related cannabinoids in artificial gastric juice, and their pharmacological effects in mice'. Forensic Toxicology. 25: 16–21. doi:10.1007/s11419-007-0021-y. S2CID2890977.
- ^Adams, Roger; Pease, D. C.; Cain, C. K.; Clark, J. H. (1940). 'Structure of Cannabidiol. VI. Isomerization of Cannabidiol to Tetrahydrocannabinol, a Physiologically Active Product. Conversion of Cannabidiol to Cannabinol'. Journal of the American Chemical Society. 62 (9): 2402–2405. doi:10.1021/ja01866a040.
- ^Adams, Roger; Cain, C. K.; McPhee, W. D.; Wearn, R. B. (1941). 'Structure of Cannabidiol. XII. Isomerization to Tetrahydrocannabinols1'. Journal of the American Chemical Society. 63 (8): 2209–2213. doi:10.1021/ja01853a052.
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