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689386
Formaldehyd-dibutylacetal
puriss., ≥97.0% (GC)
Synonym(e):
Butylal, Dibutoxymethan
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About This Item
Lineare Formel:
CH2(OCH2CH2CH2CH3)2
CAS-Nummer:
Molekulargewicht:
160.25
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualität
puriss.
Qualitätsniveau
Assay
≥97.0% (GC)
Form
liquid
Verunreinigungen
≤0.25% water
Brechungsindex
n20/D 1.406
Dichte
0.835 g/mL at 20 °C
Funktionelle Gruppe
ether
SMILES String
CCCCOCOCCCC
InChI
1S/C9H20O2/c1-3-5-7-10-9-11-8-6-4-2/h3-9H2,1-2H3
InChIKey
QLCJOAMJPCOIDI-UHFFFAOYSA-N
Verwandte Kategorien
Allgemeine Beschreibung
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.
Anwendung
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.
Lagerklassenschlüssel
10 - Combustible liquids
WGK
WGK 1
Flammpunkt (°F)
143.6 °F - closed cup
Flammpunkt (°C)
62 °C - closed cup
Persönliche Schutzausrüstung
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
Global Trade Item Number
SKU | GTIN |
---|---|
689386-1L | 4061838091291 |
689386-250ML | 4061838120670 |
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