464465
2-Butyl-1-octanol
95%
Sinônimo(s):
2-Butyloctanol, 2-Butyloctyl alcohol, 5-(Hydroxymethyl)undecane, Butyloctanol, Guerbet dodecanol
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About This Item
Fórmula linear:
CH3(CH2)5CH[(CH2)3CH3]CH2OH
Número CAS:
Peso molecular:
186.33
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
95%
p.e.
145-149 °C (lit.)
densidade
0.833 g/mL at 25 °C (lit.)
grupo funcional
hydroxyl
cadeia de caracteres SMILES
CCCCCCC(CO)CCCC
InChI
1S/C12H26O/c1-3-5-7-8-10-12(11-13)9-6-4-2/h12-13H,3-11H2,1-2H3
chave InChI
XMVBHZBLHNOQON-UHFFFAOYSA-N
Descrição geral
2-Butyl-1-octanol (BuOA) is a long-chain glass forming monohydroxy alcohol.
Aplicação
2-Butyl-1-octanol (BuOA) has been used to synthesize:
It has also been used as an extraction solvent in extractive fed-batch experiments.
- 2-butyl-1-octyl-methacrylate (BOMA)
- 3,5,5-trimethyl-1-hexyl methacrylate (TMHMA)
- hydrophobic polyesters in miniemulsion in the presence of large amounts of water
It has also been used as an extraction solvent in extractive fed-batch experiments.
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Aquatic Acute 1 - Aquatic Chronic 1
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
251.6 °F - Non-equilibrium method
Ponto de fulgor (°C)
122 °C - Non-equilibrium method
Equipamento de proteção individual
Eyeshields, Gloves
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Seven amphiphilic conetworks of methacrylic acid (MAA) and a new hydrophobic monomer, 2-butyl-1-octyl-methacrylate (BOMA), were synthesized using group transfer polymerization. The MAA units were introduced via the polymerization of tetrahydropyranyl methacrylate (THPMA) followed by the removal of the protecting tetrahydropyranyl
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Acetone/butanol/ethanol (ABE) fermentation by Clostridium acetobutylicum was investigated in extractive fed-batch experiments. In conventional fermentations, metabolic activity ceases when a critical threshold products concentration is reached (~21.6 g solvents l(-1)). Solvents production was increased up to 36.6 and 37.2 g
Yanqin Gao et al.
The Journal of chemical physics, 139(16), 164504-164504 (2013-11-05)
The dielectric relaxation of two long-chain glass forming monohydroxy alcohols, 2-butyl-1-octanol and 2-hexyl-1-decanol, is studied at low temperature. Remarkable broadening from the pure Debye relaxation is identified for the slowest dynamics, differing from the dielectric spectra of short-chain alcohols. The
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The effects of roasting, boiling, and freeze-drying after boiling on volatile aroma compounds in three varieties of Chinese foxtail millet (Setaria italica), namely, Jingu 21, Fenghonggu and Dongfangliang were determined. During boiling significant (p < 0.05) increases in the contents of several
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