689386
Formaldehyde dibutyl acetal
puriss., ≥97.0% (GC)
Sinônimo(s):
Dibutyl formal, Butylal, Dibutoxymethane
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About This Item
Fórmula linear:
CH2(OCH2CH2CH2CH3)2
Número CAS:
Peso molecular:
160.25
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
grau
puriss.
Nível de qualidade
Ensaio
≥97.0% (GC)
Formulário
liquid
Impurezas
≤0.25% water
índice de refração
n20/D 1.406
densidade
0.835 g/mL at 20 °C
grupo funcional
ether
cadeia de caracteres SMILES
CCCCOCOCCCC
InChI
1S/C9H20O2/c1-3-5-7-10-9-11-8-6-4-2/h3-9H2,1-2H3
chave InChI
QLCJOAMJPCOIDI-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
Formaldehyde dibutyl acetal is an acetal used in the manufacture of synthetic resins, antiseptics, deodorants, and fungicides. It is also used as a fuel additive to increase the octane number of gasoline or the n-cetane number of diesel fuels and reduce smoke and particulate emissions.
Aplicação
Formaldehyde dibutyl acetal is a halogen-free and less toxic solvent that can be used to solubilize commercial low-density polyethylene (LDPE) samples to analyze molecular weight distribution using gel permeation chromatography (GPC). It can also be used as a reactant to prepare butoxymethyltriphenylphosphonium iodide, which is used for carbon homologation and also as a useful key intermediate in organic synthesis.
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 1
Ponto de fulgor (°F)
143.6 °F - closed cup
Ponto de fulgor (°C)
62 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Selected physicochemical properties of dibutoxymethane
P-T Marcela and Szafranski AM
Journal of Chemical and Engineering Data, 45(6), 988-990 (2000)
Vieille-Petit, L.; et al.
Chemical Communications (Cambridge, England), 3783-3783 (2009)
Michele Gatti et al.
Journal of the American Chemical Society, 131(27), 9498-9499 (2009-06-19)
Two saturated N-heterocyclic carbene ligands with substituted naphthyl side chains were used for the preparation of Blechert-type ruthenium metathesis precatalysts. The resulting conformers of the complexes were separated and unambiguously assigned by X-ray diffraction studies. All new complexes were compared
Vieille-Petit, L.; et al.
European Journal of Inorganic Chemistry, 13, 1861-1861 (2009)
Xinjun Luan et al.
Journal of the American Chemical Society, 130(21), 6848-6858 (2008-05-01)
A new class of easily accessible and stable imidazolin-2-ylidenes has been synthesized where the side chains are comprised of substituted naphthyl units. Introduction of the naphthyl groups generates C 2 -symmetric ( rac) and C s- symmetric ( meso) atropisomers
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