Álcoois

Applications N-Acetylethanolamine can be used as an antistatic agent, foam boosting agent, hair conditioning humectant, skin conditioning surfactant and viscosity controlling agent in cosmetics industry. It is a non-tacky glycerine alternative for use in skin and hair care.
References Hough, L., et al.: J. Chem. Soc., 7923994-3997 (1957); Auzanneau, F-I, et al.: J. Chem. Soc., 10, 2831-2834 (1990);

Applications 4-Butoxybutanol is used in the synthesis of biomedical polyurethane for application as scaffold materials.
References Liu, H. et al.: J. App. Polym. Sci., 117, 235 (2010);

Applications Bis(4-diethylaminophenyl)methanol (cas# 134-91-8) is a useful research chemical.
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 2-sulfanylpropan-1-ol (cas# 3001-64-7) is a useful research chemical.

Applications (±)-2-Heptanol, is a volatile components of various plants, and can be used as flavor and fragrance ingredients. It can also be used as building block used for the synthesis of various chemicals, such as direct synthesis of pyridines and quinolines.
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 Gutierrez, D., et al.: Revista Colombiana de Quimica, 39 (3), 389 (2010); Srimani, D., et al.: Chem. Commu., 49 (59), 6632 (2013);

Applications 4-tert-Butyl-2-chlorophenol

Applications 1,7-Heptanediol is used in the treatment of cardiovascular disease. Also used in the synthesis of nonpeptidic inhibitors of human lung tryptase.
References Pepys, M. et al.: Nature. 440, 1217 (2006); Burgess, L. et al.: PNAC, 96, 8348 (1999);

Applications S-(+)-2-Amino-1-propanol is an aliphatic amino alcohol shown to induce an antiproliferative effect in B16 melanoma cells. S-(+)-2-Amino-1-propanol is used in the preparation of oxazolines which are often used as ligands in homogeneous catalysis.
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 Landau, O. et al.: Cancer Lett., 69, 203 (1993); Gant, T.G. et al.: Tetrahedron, 50, 2297 (1994);

Applications Asenapine Phenol is a research reagent used to study effect on DNA oxidation
References Bao, L.L., et al.: ChemMedChem, 11, 1617 (2016)

Applications 2,3-Dimethoxyphenol (cas# 5150-42-5) is a useful research chemical.

Applications 4-​Bromo-​3-​methyl-2-buten-1-ol is an intermediate in the synthesis of 2-[(4-Bromo-3-methyl-2-buten-1-yl)oxy]tetrahydro-2H-pyran (B681855), which is a tetrahydropyran protected intermediate used in the synthesis of L-Cysteine derivatives.

Applications 4-Mercaptophenol is used to improve charge separation in PbSe quantum dots (QDs) as sensitizers for TiO2.
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 Guijarro, N., et. al.: J. Phys. Chem. Lett., 22, 3367 (2012)

Applications 2-(3-Aminopropylamino)ethanol is the hydroxy analogue of WR-1065 (A576820), a metabolite of Amifostine (A576810). Amifostine is an organic thiophosphate that has the ability to protect a broad range of tissues from cytotoxicity (e.g. from chemotherapeutic agents) without inducing an antitumour response. 2-(3-Aminopropylamino)ethanol is also used as an nucleophilic tag in the detection of human butyrylcholinesterase adducts.
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 Antonadou, D., et al.: Int. J. Rad. Oncol. Biol. Phys., 52, 739 (2002); Kemp, G., et al.: J. Clin. Oncol., 14, 2101 (1996)

Applications 2-Cyclohexylethanol is a useful building block, and has recently been used in a green preparation of oxidative esterification of primary alcohols.
References Reddy, N.; et al.: Synth. Commun., 48, 1663 (2018).

Applications (1R,2R)-rel-trans-1,2-Cyclopentanediol is a building block for the synthesis of chiral phosphine ligands. It can also be used to prepare benzoquinolines and benzoindoles via heterocyclization of naphthylamines with diols catalyzed by iridium chloride/BINAP
References Kündig, E., et al.: Helv. Chim. Acta, 77, 421 (1994); Aramoto, H., et al.: J. Org. Chem., 74, 628 (2009)