Álcoois

Applications (4-(tert-Butyl)-1,2-phenylene)dimethanol is an intermediate in the synthesis of 4-tert-Butyl-1,2-bis(chloromethyl)benzene (B807070). 4-tert-Butyl-1,2-bis(chloromethyl)benzene is used as a reactant in the preparation of dihydronaphthalenes/naphthalenes via cobalt-catalyzed formal [4+2] cycloaddition of α,α'-dichloro-ortho-xylenes with alkynes.
References Komeyama, K., et al.: Angew. Chem. Int. Ed., 53, 11325 (2014)

Applications 2,4,4-Trimethyl-2-pentanol is an intermediate formed from incubation of Sphingomonas sp. strain with xeno-estrogenic octylphenol. It was used in study comparing the relative binding affinities of low-molecular-weight proteins from humans versus male rats.
References Tanghe, Tom., et al.: Biodegradation, 11, 11 (2000); Borghoff, S., et al.: Toxicol. Appl. Pharm., 119, 228 (1993);

Applications cis-3-Dodecen-1-ol is an intermediate for the synthesis of Z-3-Dodecenyl E-Crotonate, which can be used to develop insecticides and sex pheromone trap against Sweetpotato weevil.
References Reddy, G. V., et al.: Environ Entomol 43, 767 (2014); McQuate, G. T.: Sci Rep 4, 4499 (2014)

Applications 1-Ethynylcyclohexanol is used in the preparation of 9-methyladenines used as adenosine receptor antagonists. Also used in the cycloadition of alkynes to organic azides.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Harada, H. et al.: J. Med. Chem. 44, 170 (2001); Zhang, L. et al.: J. Am. Chem. Soc., 127, 15998 (2005);

Applications Intermediate for preparation of optically active theaspirane and β-Damascenone.
References Gertraut, S., et al.: J. Agric. Food Chem., 40, 1188 (1992), Campagnole, M., et al.: Syn. Comm., 37, 1077 (2007).

Applications 3-(2-Pentyl)phenol is an intermediate in the synthesis of Bufencarb (B689385), a carbamate pesticide used mainly as an insecticide.
References Nesterova, T.N., et al.: J. Chem. Thermodyn., 21, 385 (1989);

Applications 9-(Benzyloxy)-3,7-dimethylnona-1,7-dien-4-ol is an intermediate in the synthesis of Menaquinone 6 (M218590). Menaquinones are isoprenoid quinones of the naphthalene series and belongs to the K2 Vitamin homologs. Menaquinones were originally discovered as the anti-hemorrhagic factor and now encompasses a variety of physiological processes. Menaquinone-6 were the major isoprenoid quinones found in membrane preparations of Campylobacter jejuni and Campylobacter fetus.
References Kiesel, B., et al.: Biodegradation, 19, 435 (2008), Suhara, Y., et al.: Bioorg. Med. Chem., 16, 3108 (2008), Gast, G., et al.: Nut., Metab., Cardiovas., Diseases, 19, 504 (2009); Carlone G.M., et al.: J. Gen. Microbiol., 129, 3385 (1983);

Applications 6-Chloro-1-hexanol is used as a reagent in the synthesis of 3-(4-Chloro butyl)-1H-indole-5-carbonitrile; a key intermediate of the antidepressant drug Vilazodone (V265000).
References Anitha, N., et al.: Synthetic Commun., 44, 3563 (2014)

Applications (E)-2-Hexadecen-1-ol (cas# 26993-32-8) is a compound useful in organic synthesis.

Applications 8-Bromooctan-1-ol (cas# 50816-19-8) is a useful research chemical.

Applications 2-(4-Octylphenyl)ethanol (cas# 162358-05-6) is a compound useful in organic synthesis.

Applications 2-HEPTYN-1-OL (cas# 1002-36-4) is a useful research chemical.

Applications A substituted alkynyl phenoxy compound as new synergists in pesticidal compositions.
References Hefner,T., et al.: Bioorg. Med. Chem., 10, 1731 (2002),

Applications (2Z)-2-Penten-1-ol is one of the aroma volatiles in basil and thyme leaves with antioxidant activity.
References Lee, S., et al.: Food Chem., 91 131 (2004);

Applications 3-(Dimethylamino)-1,2-propanediol is a reagent in the synthesis of 1,2-Dioleoyl-3-trimethylammonium-propane, Chloride (D484450).
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications 1-(Phenylmethoxy)-3-(2-propen-1-yloxy)-2-propanol (cas# 83016-75-5) is a compound useful in organic synthesis.

Applications 1,3-Bis(tert-Butyldimethylsiloxy)-2-propanol is an intermediate in the synthesis of 2-Linoleoyl-rac-glycerol (L467960), which is a atty acid monoglycerides in vegetable oils with medium unsaturation.
References Compton, D., et al.: J. Pharmacol. Exp. Ther., 277, 586 (1996), Devane, W., et al.: Science, 258, 1946 (1992),

Applications 3-Hexyn-1-ol is an unsaturated alcohol that, when subjected to stereoselective hydrogenation, produces cis-3-Hexen-1-ol (H295005), a compound that is important in the fragrance industry. 3-Hexyn-1-ol also exhibits antifungal properties against Aspergillus oryzae, a fungus that is used to produce fermented foods and beverages in Japan.
References Machida, M., et al.: Nature, 438, 1157 (2005); Sachse, A., et al.: Dalt. Trans., 42, 1378 (2013); Witte, P., et al.: Stud. Surf. Sci. Catal., 175, 135 (2010)

Applications 2,4,4-Trimethyl-1-pentanol is the principal metabolite of 2,2,4-trimethylpentane (T796535), a general solvent used in organic synthesis..
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Gaur, R. et al.: Asian J. Biochem., 10, 52 (2015);

Applications 1-Butanol is a common chemical reagent used in biodiesel production. Also it has been used in the study the polarization of vapor-deposited 1-butanol films (1) as well as in the preparation of bioavailable CB1 antagonists (2) . Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References 1. Gavra, I. et al.: J. Chem. Phys. 2017 Mar 14;146(10):104701.2. Röver, S. et al.: J. Med. Chem. 2013 Dec 27;56(24):9874-96.

Applications 2-Phenyl-4-nitrosophenol is an intermediate in the synthesis of (E)-2-((6-Hydroxy-[1,1'-biphenyl]-3-yl)((6-hydroxy-[1,1'-biphenyl]-3-yl)imino)methyl)benzoic Acid which is an impurity of (S)-Cloperastine (C587195); a drug used in the treatment of chronic non-productive cough. Also antitussive.
References Aliprandi, P. et al.: Drugs Exp. Clin. Res., 30, 133 (2004); Aliprandi, P. et al.: Clin. Drug Invest. 22, 209 (2002)

Applications (1R,2R)-1,2-Cyclopentanedimethanol is an intermediate in the synthesis of trans-1,2-Dimethylcyclopentane (D464925). trans-1,2-Dimethylcyclopentane was found in sedimentary rocks and was one of the hydrocarbons used to determine its maturation history.
References Schaefer, R.G., Littke, R.: Org. Geochem., 13, 887 (1988)

Applications 10-Amino-1-decanol (cas# 23160-46-5) is a compound useful in organic synthesis.
References Lee, T., et al.: J. Biol. Chem., 270, 5375 (1995),

Applications (±)-3-Heptanol, is a volatile components of various plants, and can be used as flavor and fragrance ingredients. It is also used as building block used for the synthesis of various chemicals. It is used for the preparation of biologically active ester derivatives as potent inhibitors of the soluble epoxide hydrolase.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Kim, I., et al.: Bioorg. Med. Chem. Lett., 55 (18), 5889 (2012); Gibka, J., et al.: Zeszyty Naukowe - Politechnika Lodzka, 60, 65 (1998);

Applications rac 1-O-Trimethylsilyl 3-Chloro-1,2-propanediol (cas# 1246820-26-7) is a compound useful in organic synthesis.

Applications 5-(4-Hydroxypentyl)-1,3-benzenediol is an intermediate used in the synthesis of 4''-Hydroxycannabidiol (H824830), which is a metabolite of Canabidiol (C175300), a major constituents in marijuana. 4''-Hydroxycannabidiol be used to investigate canabidiol metabolism and human liver microsomes that metabolize Canabidiol into 6α-Hydroxycannabidiol.
References Jiang, R., et al.: Life Sci. 89, 165 (2011); Lander, N., et al.: Science 169, 611 (1970)

4-Mercaptobenzyl alcohol (MBBA) is a bifunctional molecule that can act as an electron donor and electron acceptor. It has been shown to have proapoptotic activity, which may be due to its ability to interact with cellular components and induce DNA damage. MBBA has also been shown to inhibit the growth of bacteria by attacking their cell walls and inhibiting their ability to synthesize proteins. The antibacterial activity of MBBA was found to be enhanced on metal surfaces, such as aluminum and copper, which are commonly used in cancer therapy equipment or for antimicrobial resistance. MBBA also has diagnostic properties, which can be used for the detection of cancer cells or bacterial infections.
MBBA is absorbed into cells through the carboxylate groups on the surface of the cell membrane. Electrons are then transferred from the molecule to the cell's electron transport chain, thereby increasing ATP production and inducing apoptosis in cancer cells.

8-Methoxycarbonyloctanol (8MCO) is a fatty acid molecule that has been shown to have significant inhibitory activities against Streptococcus pneumoniae in human serum. 8MCO is a synthetic molecule that can be synthesized from galactose and chloride. It has been found to have a molecular weight of 190.08 g/mol, melting point of -2°C, and boiling point of 217°C at 1 mmHg. 8MCO is soluble in water, methanol, and ethanol. This molecule can be used as an analytical tool for the detection of fatty acids by gas chromatography-mass spectrometry (GC-MS). It also exhibits enzymatic activity when incorporated into enzyme preparations such as esterases and lipases. 8MCO contains functional groups such as carbonyl (-CO), hydroxyl (-OH), carboxylic acid (-COOH), ether (-O-) and alcohol (-

3-(1,1,2,2-Tetrafluoroethoxy)phenol is a versatile building block that can be used in the synthesis of complex compounds. It is also a reagent and speciality chemical and has CAS No. 53997-99-2. 3-(1,1,2,2-Tetrafluoroethoxy)phenol is a useful building block for organic synthesis and has been used as a reaction component or scaffold.

17alpha-Hydroxypregnenolone is a steroid hormone that has been shown to have effects on the metabolism of lipids, glucose and protein. This compound is synthesized from progesterone by the enzyme 17alpha-hydroxylase and is converted to 17beta-hydroxyprogesterone by the enzyme 17,20 lyase. It has been shown to have an effect on body mass index in humans and model organisms such as mice. The tissue culture studies showed that 17alpha-Hydroxypregnenolone led to an increase in serum bile acids. In adrenocortical carcinoma cell lines, this compound was found to inhibit the growth of cancer cells through inhibition of DNA synthesis and protein synthesis through inhibition of RNA polymerase II activity. It also inhibits infectious diseases by decreasing virus production and increasing the production of interferon alpha. When synthesized for use in experimental models, this compound can be used as a marker for metabolic disorders or cation

Pycnogenol is a nonsteroidal anti-inflammatory drug that is derived from the bark of the French maritime pine tree. It has been shown to reduce bowel disease activity in animal models and has been found to be as effective as ibuprofen in human studies. Pycnogenol also inhibits the expression of toll-like receptor 4, which reduces inflammation in cells. Pycnogenol has also been shown to have an anti-inflammatory effect on human polymorphonuclear leukocytes and may be useful for treating various diseases such as cancer, cardiovascular diseases, or asthma. This compound also has natural antioxidant properties that are thought to protect against oxidative damage and help regulate blood pressure by inhibiting vascular smooth muscle proliferation.

Phloroglucinol dihydrate is a chemical substance that can be used as a denaturant, conditioner and deodorant. It is soluble in water and has been shown to have enzyme-inhibiting properties. Phloroglucinol dihydrate has been shown to have anti-inflammatory properties by inhibiting the production of prostaglandins. This compound also has optical properties, which are determined by its chromene structure. There is no phase transition temperature for this compound because it does not melt or freeze.

2-Bromo-4-methylphenol is an organic compound that has interactive effects with hydrochloric acid, molybdenum, and trifluoromethanesulfonic acid. It is soluble in water vapor, but insoluble in polyvinyl. 2-Bromo-4-methylphenol reacts with sodium hydroxide solution to form a hydroxide solution and sodium carbonate. The reaction product of 2-bromo-4-methylphenol with triterpenoid saponin produces fatty acids. This reaction occurs because the hydroxide ion from the sodium hydroxide solution attacks the ester group of the saponin, forming an alcohol group on one end and a carboxylic acid group on the other end. The benzyl groups are removed by hydrogenation to produce phenol.

2-(2-Bromophenyl)ethanol is a functional group that contains a bromine atom and an ethoxy group. This compound is used to synthesize condensation products, such as the crystal x-ray diffraction of crystallized palladium complexes with acetaldehyde. The 2-(2-bromophenyl)ethanol analog was synthesized in order to study the synthesis and reactivity of a chelate ring. The hydroxyl group on this compound is useful for forming a magnesium salt or for using it as a synthetic reagent.

3-(Trifluoromethoxy)phenol is a drug that has been shown to function as an amide and a biomolecular. It has also been used in the development of drugs for depression, but it is not known whether it is effective in humans. 3-(Trifluoromethoxy)phenol binds to the cation channel of the NMDA receptor, which may be related to its antidepressant properties. The compound has been shown to have a radiotracer effect on positron emission tomography (PET). 3-(Trifluoromethoxy)phenol yields positrons when it undergoes deamination. This reaction is catalyzed by enzymes such as acetylcholine esterase, choline oxidase, and monoamine oxidases.

1-Naphthalene ethanol is a stabilizer that is used in the alkaline hydrolysis of primary amines. It has been shown to have fluorescence activity and has been used as a dye intermediate and chemical intermediate. 1-Naphthalene ethanol has also been shown to be an acetylation, ethylene, and dehydration agent. The compound is also a particle stabilizer and can be used as an additive for fuels. 1-Naphthalene ethanol is also a reagent that can transfer amines onto acidic chloride or chloral compounds.

Deoxynivalenol is a mycotoxin that is produced by the fungi Fusarium graminearum and F. culmorum. It produces toxic effects in humans and animals, including human immunoglobulin E (IgE) production, acute toxicities, and cytotoxic effects on cultured human leukocytes. The analytical method for deoxynivalenol detection includes a variety of in vitro methods such as enzyme-linked immunosorbent assays (ELISA), competitive ELISA, fluorescent antibody staining assay, fluorescence polarization immunoassay (FPIA), competitive FPIA, and high performance liquid chromatography (HPLC). Deoxynivalenol binds to dna with high affinity and has been shown to have fusarial activity. The toxicity of deoxynivalenol can be confirmed by the mitochondrial membrane potential assay or by the assessment of vomitoxin levels. Colloidal gold can be used for identification of deox

Quinoline-2,8-diol is a bacterial strain that can be used to remove fatty acids from wastewater. The recombinant cytochrome P450 in this strain can degrade fatty acids, which are carcinogenic and have been shown to cause hepatic steatosis. In addition, the quinoline-2,8-diol strain has shown an ability to inhibit xenograft tumor growth in mice by activating cytochrome P450 and inducing apoptosis. This bacterial strain also has the potential to produce xanthurenic acid from tyrosine. Xanthurenic acid is toxic and has been shown to inhibit polymerase chain reaction (PCR) amplification of DNA. Quinoline-2,8-diol may be used as a model for experimental studies of xanthurenic acid's effects on energy metabolism and DNA synthesis.

Quinoline-5-carboxylic acid is a peroxide that is produced by the oxidation of quinoline derivatives. Quinoline-5-carboxylic acid has been shown to have antibacterial activity, and it also has affinity values for chloride ions. The chemical isomers of quinoline-5-carboxylic acid are called quninolines, which are produced by the hydrolysis of quinoline-5-carboxylic acid. Quinolines can be obtained by the oxidation of aniline. Quinolines have been shown to catalyze reactions with carbonyl groups in organic molecules, such as the reaction between an alkoxycarbonyl group and a hydroxyl group to form an aldehyde or ketone. Kinetic data for this reaction was obtained using titration calorimetry.