1-hydroxy-4-unsubstituted benzenoids
Sigma Aldrich Fine Chemicals Biosciences 4-Ethylphenol >=98%, FG | 123-07-9 | MFCD00002393 |
4-Ethylphenol >=98%, FG | Purity: >=98% | Mol Wt: 122.16 | 123-07-9 | MFCD00002393 |
eMolecules 2-Chloro-n-(3-hydroxyphenyl)acetamide | 10147-69-0 | MFCD00709261 | 1g
Combi-Blocks | 2-Chloro-n-(3-hydroxyphenyl)acetamide | 1g | 528670281 | QY-8701 | 97.000 | 10147-69-0 | MFCD00709261 | 185.610 | C8H8ClNO2
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eMolecules 4-(3-Fluoro-4-hydroxyphenyl)phenol | 885473-84-7 | MFCD18312816 | 1g
Combi-Blocks | 4-(3-Fluoro-4-hydroxyphenyl)phenol | 1g | 117578066 | YA-1554 | 96.000 | 885473-84-7 | MFCD18312816 | 204.200 | C12H9FO2
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Medchemexpress LLC 1-Indanone | 83-33-0 | 132.16 | 250 G
This biochemical reagent is a light yellow to brown solid. It is primarily used in life science research as a biological material or organic compound. It has a molecular weight of 132.16 and a purity of 99.9%. As an oxidation product, it is found in fuels, solvents, and varnishes. It plays a role in steroid hormone biosynthesis and arachidonic acid metabolism pathways.
- Biochemical reagent for life science research
- Organic compound for research purposes
- Involved in steroid hormone biosynthesis
- Participates in arachidonic acid metabolism pathways
Medchemexpress LLC 1-Indanone | 83-33-0 | 132.16 | 100 G
1-Indanone is a biochemical reagent suitable for life science research. It serves as a biological material or organic compound and is an oxidation product. This compound is also a component found in fuels, solvents, and varnishes. Additionally, it is involved in steroid hormone biosynthesis and arachidonic acid metabolism pathways.
- Used in life science research
- Can be used as a biological material
- Can be used as an organic compound
- Functions as an oxidation product
- Component of fuels, solvents, and varnishes
- Involved in steroid hormone biosynthesis pathways
- Involved in arachidonic acid metabolism pathways
Medchemexpress LLC 1-Indanone | 83-33-0 | 132.16 | 500 G
1-Indanone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. It is an oxidation product and a component of fuels, solvents, and varnishes. It is also involved in steroid hormone biosynthesis and arachidonic acid metabolism pathways.
- Used as a biological material
- Used as an organic compound for life science research
- An oxidation product
- Component of fuels, solvents, and varnishes
- Involved in steroid hormone biosynthesis pathways
- Involved in arachidonic acid metabolism pathways
Apexbio Technology LLC 4-Ethylphenol 123-07-9 100mg
4-Ethylphenol (CAS 123-07-9) is a volatile phenolic compound predominantly produced through the microbial decarboxylation and reduction of p-coumaric acid during fermentation and other metabolic processes It is frequently utilized to investigate the microbial enzymatic pathways underlying aromatic compound metabolism In biomedical research 4-ethylphenol serves as a model molecule for studying the interplay between microbial metabolites and host metabolic networks as well as for the identification of microbial biomarkers in health and disease Its applications extend to experiments addressing the dynamics of microbial communities and host-microbe interactions
Medchemexpress LLC 4-Ethylphenol | 123-07-9 | 100.0% | 122.17 | 25 G
4-Ethylphenol | 123-07-9 | 100.0% | 122.17 | 25 G
Accela Chembio Inc 1-(3-hydroxyphenyl)ethanol | 25g | 2415-09-0 | MFCD00238621 | 97+% | Shelf Life: 1260 Days | Regular
1-(3-hydroxyphenyl)ethanol | 25g | 2415-09-0 | MFCD00238621 | 97+% | Shelf Life: 1260 Days | Regular
Medchemexpress LLC 4-Ethylphenol | 123-07-9 | 99.99% | 122.17 | 50 G
4-Ethylphenol is a volatile phenolic compound associated with off-odour in wine. It is a phenolic compound that can be synthesized by intestinal flora and is converted to 4-ethylphenyl sulfate by Lactobacillus plantarum.
- Causes DNA damage and induces the formation of 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxodG) in calf thymus DNA under the presence of Cu (II).
- Reduces oligodendrocyte maturation and myelination in brains.
- Causes increased anxiety-like behavior in C57BL/6J mouse models.
- Causes mortality during labor and in offspring in Sprague Dawley rat models.
- Leads to some abnormal nursing behaviors in Sprague Dawley rat models.
Medchemexpress LLC 4-Hydroxy-1-indanone | 40731-98-4 | 148.16 | 25 G
4-Hydroxy-1-indanone is a biochemical reagent designed for life science research. This organic compound is intended for research use only and not for patient application.
- Biochemical reagent
- Used as a biological material or organic compound for life science related research
- For research use only
- Solid appearance
- Soluble in DMSO (100 mg/mL)
Chemscene ChemScene | tert-Butyl (2-hydroxyphenyl)carbamate | 1G | CS-0031385 | 0.98 | 186663-74-1| MFCD06411300 | 209.25
ChemScene | tert-Butyl (2-hydroxyphenyl)carbamate | 1G | CS-0031385 | 0.98 | 186663-74-1| MFCD06411300 | 209.25
eMolecules 4-(3-Fluoro-4-hydroxyphenyl)benzoic acid | 106291-26-3 | MFCD00994624 | 1g
Combi-Blocks | 4-(3-Fluoro-4-hydroxyphenyl)benzoic acid | 1g | 117577201 | YA-1074 | 95.000 | 106291-26-3 | MFCD00994624 | 232.210 | C13H9FO3
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Selleck Chemical LLC 2-O-a-D-Glucopyranosyl-L-ascorbic acid S3215-5mg
2-O- -D-Glucopyranosyl-l-ascorbic acid (AA-2G) which is a glucoside derivative of ascorbic acid (AA) shows vitamin C activity after enzymatic hydrolysis to ascorbic acid The antitumor activity of AA-2G is caused by ROS generated by AA released by rapid hydrolysis of AA-2G