Isoeugenol,mixture of cis and trans
Isoeugenol,mixture of cis and trans structure
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Common Name | Isoeugenol,mixture of cis and trans | ||
|---|---|---|---|---|
| CAS Number | 97-54-1 | Molecular Weight | 164.201 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 266.6±20.0 °C at 760 mmHg | |
| Molecular Formula | C10H12O2 | Melting Point | -10 °C | |
| MSDS | Chinese USA | Flash Point | 122.9±6.7 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Parallel dual secondary column-dual detection: a further way of enhancing the informative potential of two-dimensional comprehensive gas chromatography.
J. Chromatogr. A. 1360 , 264-74, (2014) Comprehensive two-dimensional gas chromatography (GC×GC) coupled with Mass Spectrometry (MS) is one of today's most powerful analytical platforms for detailed analysis of medium-to-high complexity samples. The column set usually consists of a long, convention... |
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Impact of eugenol and isoeugenol on AhR translocation, target gene expression, and proliferation in human HaCaT keratinocytes.
J. Toxicol. Environ. Health A 75(8-10) , 478-91, (2012) The phenolic derivatives eugenol and isoeugenol, which are naturally found in essential oils of different spices, are commonly used as fragrances. Recently data demonstrated that growth suppression produced by these substances occurs in keratinocytes and that... |
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In chemico evaluation of skin metabolism: Investigation of eugenol and isoeugenol by electrochemistry coupled to liquid chromatography and mass spectrometry.
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 913-914 , 106-12, (2013) Skin sensitization is initiated by the modification of proteins located in the skin. After oxidative activation, eugenol and isoeugenol have the potential to modify skin proteins and therefore cause sensitization processes. Despite their known skin sensitizin... |
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IL-8 release from human neutrophils cultured with pro-haptenic chemical sensitizers.
Chem. Res. Toxicol. 25(10) , 2054-6, (2012) Cytokine release from dendritic cells in vitro is a useful marker to discriminate between sensitizing and irritant haptenic chemicals. Unfortunately, pro-haptens, which gain reactivity following metabolic/auto activation, yield negative results. To overcome t... |
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Ultraviolet-tunable laser induced phototransformations of matrix isolated isoeugenol and eugenol.
J. Phys. Chem. B 116(36) , 11148-58, (2012) In situ photochemical transformations of monomers of 2-methoxy-4-(prop-1-enyl)phenol (isoeugenol) and 2-methoxy-4-(prop-2-enyl)phenol (eugenol) isolated in low temperature matrices were induced by tunable UV laser light, and the progress of the reactions was ... |
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Allyl/propenyl phenol synthases from the creosote bush and engineering production of specialty/commodity chemicals, eugenol/isoeugenol, in Escherichia coli.
Arch. Biochem. Biophys. 541 , 37-46, (2014) The creosote bush (Larrea tridentata) harbors members of the monolignol acyltransferase, allylphenol synthase, and propenylphenol synthase gene families, whose products together are able to catalyze distinct regiospecific conversions of various monolignols in... |
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Conversion of isoeugenol to vanillin by Psychrobacter sp. strain CSW4.
Appl. Biochem. Biotechnol. 166(1) , 1-12, (2012) To screen strains of halotolerant or halophile bacteria which are able to convert isoeugenol to vanillin, 36 different strains of bacteria isolated from the salty environments in Iran were investigated. During growth on isoeugenol, a moderately halotolerant G... |
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Evaluation of antiarthritic activity of isoeugenol in adjuvant induced arthritis in murine model.
Food Chem. Toxicol. 50(8) , 2689-95, (2012) Isoeugenol, a component of clover oil, possesses potent anti-inflammatory and antioxidant activity. In the present study, we investigated the effect on experimentally induced adjuvant arthritis in rats. Induction of arthritis in adjuvant exposed rats was conf... |
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Isoeugenol-based novel potent antioxidants: synthesis and reactivity.
Eur. J. Med. Chem. 46 , 4618-24, (2011) We are attempting to develop the novel phenolic synthetic antioxidants aimed at retarding the effects of free radicals and oxidants. The phenolic compounds (7-12) were synthesized by Friedel-Crafts alkylation of isoeugenol (1) and phenol derivatives (2-6) and... |
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Encapsulating contact allergens in liposomes, ethosomes, and polycaprolactone may affect their sensitizing properties.
Cutan. Ocul. Toxicol. 30(2) , 116-23, (2011) Attempts to improve formulation of topical products are a continuing process and the development of micro- and nanovesicular systems as well as polymeric microparticles has led to marketing of topical drugs and cosmetics using these technologies. Encapsulatio... |