1173021-20-9
1173021-20-9
Chemical Structure
4-tert-Octylphenol-3,5-d2
Synonym(s): p-Octylphenol-d2
- CAS No.: 1173021-20-9
- Formula:C14H20D2O
- Molecular Weight:208.34
IUPAC Name: 4-(2,4,4-trimethylpentan-2-yl)phen-3,5-d2-ol
InChIKey: ISAVYTVYFVQUDY-QFIQSOQBSA-N
SMILES: CC(C)(C)CC(C)(C1=C([2H])C=C(C=C1[2H])O)C
Biological Activity: 4-tert-Octylphenol-3,5-d2 is the deuterium labeled 4-tert-Octylphenol-3,5[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-tert-Octylphenol-3,5-d2 | 4-tert-Octylphenol-3,5-d2 is the deuterium labeled 4-tert-Octylphenol-3,5. | |||||||||||||||||||||
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4-tert-Octylphenol (Standard) | ≥98% | 4-tert-Octylphenol (Standard) is the analytical standard of 4-tert-Octylphenol. This product is intended for research and analytical applications. 4-tert-Octylphenol, a endocrine-disrupting chemical, is an estrogenic agent. 4-tert-Octylphenol is also a biodegradation product of non-ionic surfactants alkylphenol polyethoxylates. 4-tert-Octylphenol induces apoptosis in neuronal progenitor cells in offspring mouse brain. 4-tert-Octylphenol reduces bromodeoxyuridine (BrdU), mitotic marker Ki67, and phospho-histone H3 (p-Histone-H3), resulting in a reduction of neuronal progenitor proliferation. 4-tert-Octylphenol disrupts brain development and behavior in mice, which is promising for reserch of immune response, neuro-related diseases and ethology. | ||||||||||||||||||||
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4-tert-Octylphenol-13C6 | 4-tert-Octylphenol-13C6 is the 13C labeled isotope of Octylphenol. | |||||||||||||||||||||
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4-tert-Octylphenol | 99.70% | 4-tert-Octylphenol, a endocrine-disrupting chemical, is an estrogenic agent. 4-tert-Octylphenol is also a biodegradation product of non-ionic surfactants alkylphenol polyethoxylates. 4-tert-Octylphenol induces apoptosis in neuronal progenitor cells in offspring mouse brain. 4-tert-Octylphenol reduces bromodeoxyuridine (BrdU), mitotic marker Ki67, and phospho-histone H3 (p-Histone-H3), resulting in a reduction of neuronal progenitor proliferation. 4-tert-Octylphenol disrupts brain development and behavior in mice, which is promising for reserch of immune response, neuro-related diseases and ethology. | ||||||||||||||||||||
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2,4-Di-tert-butylphenol (Standard) | 99.67% | 2,4-Di-tert-butylphenol (Standard) is the analytical standard of 2,4-Di-tert-butylphenol (HY-W014589). This product is intended for research and analytical applications. 2,4-Di-tert-butylphenol (2,4-DTBP) is an orally active RXRα activator and a human estrogen receptor ligand with anti-inflammatory and antioxidant activities, which can induce apoptosis in tumor cells. 2,4-Di-tert-butylphenol can activate the RXRα subtype in LXRα/RXRα, PPARγ/RXRα, and hormone receptor β/RXRα. 2,4-Di-tert-butylphenol also has antiviral and antifungal activities, and has the potential to inhibit Aβ-induced neurotoxicity. 2,4-Di-tert-butylphenol can be used as an intermediate in the preparation of antioxidants and UV stabilizers, and is also used in the manufacture of pharmaceuticals and fragrances. | ||||||||||||||||||||
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Lilial | 99.49% | Lilial is a widely used synthetic fragrance and ester in consumer products. Lilial possesses estrogenic activity in vitro. Lilial can induce a toxic effect on mitochondria that causes a decrease in the viability of HaCaT cells. Lilial can increase NRF2 protein level in vitro. Lilial is able to target respiratory chain complexes, inhibit complexes I and II of the electron transport chain, increase the generation of reactive oxygen species, and decrease the level of intracellular ATP. Lilial can induce systemic toxicity in vivo. Lilial induces significant DNA strand breaks. | ||||||||||||||||||||
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3,5-Di-tert-butylphenol | 99.91% | 3,5-Di-tert-butylphenol is an volatile organic compound with anti-biofilm and antifungal activities. 3,5-Di-tert-butylphenol induces accumulation of reactive oxygen species (ROS) in C. albicans cells. 3,5-Di-tert-butylphenol also has antibacterial activities. | ||||||||||||||||||||
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1,4-Di-tert-butylbenzene | 1,4-Di-tert-butylbenzene is a volatile compound identified in the hexane extracts of corn cob and green millet. 1,4-Di-tert-butylbenzene shows potent inhibition against receptor proteins of Bacterial type II topoisomerase (4PLB and LpxC) in docking analysis. | |||||||||||||||||||||
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4-tert-Amylphenol | 99.50% | 4-tert-Amylphenol is the hydrolysis product of the mixture of phosphorous acid 2,4-bis (1,1-dimethylpropyl) phenyl ester and phosphorous acid 4-(1,1-dimethylpropyl) phenyl triester. | ||||||||||||||||||||
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p-Cymen-8-ol | p-Cymen-8-ol is an alcohol. p-Cymen-8-ol can be used to make essential oils. Essential oils containing p-Cymen-8-ol exhibit immunomodulatory activity. p-Cymen-8-ol, when used in combination with other substances to make essential oils, exerts an anxiolytic-like effect and reduces hepatic lipid peroxidation levels in ICR mice. p-Cymen-8-ol may be used in research on anxiolytic and other neurological and immune system disorders. | |||||||||||||||||||||
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4′-tert-Butylacetophenone (Standard) | ≥98% | 4′-tert-Butylacetophenone (Standard) is the analytical standard of 4′-tert-Butylacetophenone. This product is intended for research and analytical applications. 4′-tert-Butylacetophenone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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3-t-Butylphenol | 99.37% | 3-t-Butylphenol is a mitochondrial uncoupler. 3-t-Butylphenol disrupts the proton gradient, inhibits ATP synthesis and induces cytotoxicity. | ||||||||||||||||||||
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