10 Results for "

volatile oxidation compounds

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "volatile oxidation compounds" in MCE Product Catalog:

Cat. No.: HY-W015777
CAS No.: 105-13-5
Synonyms: P-Methoxy-benzyl alcoho; (4-Methoxyphenyl)methanol
4-Methoxybenzyl alcohol (P-Methoxy-benzyl alcoho; (4-Methoxyphenyl) methanol) is a naturally derived volatile aromatic compound. 4-Methoxybenzyl alcohol upregulates the phosphorylation level of PI3K/Akt pathway proteins, downregulates the expression of pro-inflammatory factors, increases the content of tight junction proteins occludin and claudin-5, and alleviates structural damage to the blood-brain barrier. 4-Methoxybenzyl alcohol improves the decrease in viability and NO level of cerebral microvascular endothelial cells induced by oxygen-glucose deprivation/reperfusion, and reduces the release of lactate dehydrogenase. 4-Methoxybenzyl alcohol serves as a substrate in the two-phase persulfate-mediated electro-oxidation system, where it is directionally oxidized to p-anisaldehyde. 4-Methoxybenzyl alcohol acts as a substrate for wild-type fungal aryl alcohol oxidase. 4-Methoxybenzyl alcohol can be used in studies related to ischemic stroke, as well as in research across various fields such as chemical synthesis, including the synthesis of fragrances and flavorings .
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Cat. No.: HY-W015810
CAS No.: 617-94-7
2-Phenyl-2-propanol is a volatile signaling compound released by rhizosphere microorganisms, and also a key product of the selective oxidation of cumene. 2-Phenyl-2-propanol alters primary root structure, regulates the expression of auxin and (±)-Jasmonic acid (HY-122464) responsive genes, and affects cell division. 2-Phenyl-2-propanol reduces the primary root length, lateral root number, lateral root density, and aboveground fresh weight of *Arabidopsis thaliana*. 2-Phenyl-2-propanol is commonly used in research related to cosmetics, pesticides, pharmaceuticals and other fields .
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Cat. No.: HY-W102525
CAS No.: 16409-43-1
Target:  

Drug Derivative

Research Areas:  

Others

Rose oxide is a kind of monoterpenoid volatile organic compound with a distinctive rose fragrance. However, rose oxide does not have inhibitory activity against the formation of breast cancer stem cells .
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Cat. No.: HY-N11526
CAS No.: 14015-55-5
Category:  

Lipids

Target:  

Others

3-Hydroxy-2-(palmitoyloxy)propyl stearat is a non-volatile compound. 3-Hydroxy-2-(palmitoyloxy)propyl stearat can be isolated from less polar fractions of the brown macroalga Fucus virsoides J. Agardh. This part of the substance has a good ability to scavenge free radicals and has a protective effect on the oxidative stress induced by hydrogen peroxide in zebrafish embryos .
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Cat. No.: HY-W015777R
CAS No.: 105-13-5
Synonyms: P-Methoxy-benzyl alcoho (Standard); (4-Methoxyphenyl)methanol (Standard)
4-Methoxybenzyl alcohol (Standard) (P-Methoxy-benzyl alcoho (Standard); (4-Methoxyphenyl)methanol (Standard)) is the analytical standard of 4-Methoxybenzyl alcohol (HY-W015777). This product is intended for research and analytical applications. 4-Methoxybenzyl alcohol (P-Methoxy-benzyl alcoho; (4-Methoxyphenyl) methanol) is a naturally derived volatile aromatic compound. 4-Methoxybenzyl alcohol upregulates the phosphorylation level of PI3K/Akt pathway proteins, downregulates the expression of pro-inflammatory factors, increases the content of tight junction proteins occludin and claudin-5, and alleviates structural damage to the blood-brain barrier. 4-Methoxybenzyl alcohol improves the decrease in viability and NO level of cerebral microvascular endothelial cells induced by oxygen-glucose deprivation/reperfusion, and reduces the release of lactate dehydrogenase. 4-Methoxybenzyl alcohol serves as a substrate in the two-phase persulfate-mediated electro-oxidation system, where it is directionally oxidized to p-anisaldehyde. 4-Methoxybenzyl alcohol acts as a substrate for wild-type fungal aryl alcohol oxidase. 4-Methoxybenzyl alcohol can be used in studies related to ischemic stroke, as well as in research across various fields such as chemical synthesis, including the synthesis of fragrances and flavorings .
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Cat. No.: HY-W540405
CAS No.: 3404-72-6
2,3-Dimethyl-1-pentene is volatile compound produced by the thermal oxidation of Cholesterol (HY-N0322) .
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Cat. No.: HY-76217
CAS No.: 823-82-5
Synonyms: 2,5-Diformylfuran
Target:  

Drug Derivative

2,5-Furandicarboxaldehyde (2,5-Diformylfuran), a furan derivative, is a volatile organic compound. 2,5-Furandicarboxaldehyde the aerobic oxidation product of 5-Hydroxymethylfurfural (HY-Y0051), and can be used in organic synthesis and functional polymer manufacture, such as fluorescent material, surfactants, and vitrimer .
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Cat. No.: HY-W585888
CAS No.: 87304-79-8
Research Areas:  

Others

Fructose-isoleucine is a non-volatile Amadori compound and Maillard reaction intermediate. Fructose-isoleucine is associated with roasted flavor and roasted odor in chicken soup samples as well as chicken soup supplemented with yeast-derived flavor products. Fructose-isoleucine is formed via the amino-carbonyl reaction and induces oxidative browning in miso, white wine and Saké. In malt, Fructose-isoleucine acts as a precursor via Strecker degradation to generate flavor compounds with roasted and sweet aromas .
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Cat. No.: HY-N21799
CAS No.: 64190-80-3
Hexadecyl ferulate is a lipophilic C16 alkyl ferulate synthesized from ferulic acid and cetyl alcohol, possessing free radical-scavenging antioxidant activity . Hexadecyl ferulate inhibits the formation of lipid oxidation products in soybean oil during deep frying and exhibits antioxidant efficacy that increases with alkyl chain length. Hexadecyl ferulate can be used in antioxidant-related research .
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Cat. No.: HY-W015810R
CAS No.: 617-94-7
2-Phenyl-2-propanol (Standard) is the analytical standard of 2-Phenyl-2-propanol (HY-W015810). This product is intended for research and analytical applications. 2-Phenyl-2-propanol is a volatile signaling compound released by rhizosphere microorganisms, and also a key product of the selective oxidation of cumene. 2-Phenyl-2-propanol alters primary root structure, regulates the expression of auxin and (±)-Jasmonic acid (HY-122464) responsive genes, and affects cell division. 2-Phenyl-2-propanol reduces the primary root length, lateral root number, lateral root density, and aboveground fresh weight of *Arabidopsis thaliana*. 2-Phenyl-2-propanol is commonly used in research related to cosmetics, pesticides, pharmaceuticals and other fields .
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