176958
Propionaldehyde diethyl acetal
97%
Synonym(s):
1,1-Diethoxypropane
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
CH3CH2CH(OC2H5)2
CAS Number:
Molecular Weight:
132.20
Beilstein:
1697731
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.389 (lit.)
bp
122.8 °C (lit.)
density
0.815 g/mL at 25 °C (lit.)
functional group
ether
SMILES string
CCOC(CC)OCC
InChI
1S/C7H16O2/c1-4-7(8-5-2)9-6-3/h7H,4-6H2,1-3H3
InChI key
MBNMGGKBGCIEGF-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
Propionaldehyde diethyl acetal was used as a reducing agent in the aerobic epoxidation of alkenes.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
53.6 °F - closed cup
Flash Point(C)
12 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Co (thd)2: a superior catalyst for aerobic epoxidation and hydroperoxysilylation of unactivated alkenes: application to the synthesis of spiro-1, 2, 4-trioxanes.
Tetrahedron Letters, 44(44), 8135-8138 (2003)
Rita De Santis et al.
PloS one, 6(6), e21075-e21075 (2011-06-28)
We recently reported that the oxidized avidin, named AvidinOX®, resides for weeks within injected tissues as a consequence of the formation of Schiff's bases between its aldehyde groups and tissue protein amino groups. We also showed, in a mouse pre-clinical
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service