385395
Acetaldehyde dimethyl acetal
95%
Synonym(s):
1,1-Dimethoxyethane, Dimethyl acetal
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About This Item
Linear Formula:
CH3CH(OCH3)2
CAS Number:
Molecular Weight:
90.12
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39021102
UNSPSC Code:
12352100
EC Number:
208-589-8
MDL number:
Beilstein/REAXYS Number:
1697039
Product Name
Acetaldehyde dimethyl acetal, 95%
InChI key
SPEUIVXLLWOEMJ-UHFFFAOYSA-N
InChI
1S/C4H10O2/c1-4(5-2)6-3/h4H,1-3H3
SMILES string
COC(C)OC
vapor density
3.1 (vs air)
assay
95%
form
liquid
refractive index
n20/D 1.367 (lit.)
bp
64 °C (lit.)
density
0.852 g/mL at 25 °C (lit.)
functional group
acetal
ether
Quality Level
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Application
Acetaldehyde dimethyl acetal may be used in the preparation of glucoside derivatives of steganol. It may be used as polymer solvent for the encapsulation of water-soluble model protein, bovine serum albumin into biodegradable poly(D,L-lactic acid.
General description
Kinetics of oxidative degradation of acetaldehyde dimethyl acetal has been studied by pulse radiolysis. It also undergoes addition with various ketones, esters, amides and thioesters in the presence of silyl trifluoromethanesulfonates and an amine base. Lewis acid-mediated reaction of the titanium enolate of (S)-N-acetyl-4-isopropyl-1,3-thiazolidine-2-thione with acetaldehyde dimethyl acetal has been studied.
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
1.4 °F - closed cup
flash_point_c
-17 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Regulatory Information
危险化学品
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Hydroxyl-radical-induced oxidation of acetaldehyde dimethyl acetal in oxygenated aqueous solution. Rapid O2 anion radical release from the MeC (OMe)2O2 radical.
Schuchmann MN, et al.
Journal of the American Chemical Society, 112(1), 403-407 (1990)
Enantiopure β-methoxy carboxyl derivatives from a chiral titanium enolate and dimethyl acetals.
Cosp A, et al.
Tetrahedron Letters, 42(28), 4629-4631 (2001)
R P Hicks et al.
Journal of natural products, 48(3), 357-362 (1985-05-01)
Glucoside derivatives of steganol analogous to the semisynthetic podophyllotoxin derivative, VP 16-213, were prepared. Glucosidation of steganol with 2, 3, 4, 6-tetra-O-benzylglucopyranose gave the alpha-anomer of the glucoside as the major product. Subsequent removal of the benzyl groups and reaction
B Gander et al.
Journal of microencapsulation, 12(1), 83-97 (1995-01-01)
The aim was to study the effect of the type of polymer solvent on characteristics of microspheres produced by spray drying. The water-soluble model protein, bovine serum albumin (BSA) was microencapsulated into biodegradable poly(D,L-lactic acid) using the following 10 different
A Chandra et al.
Lipids, 32(7), 779-782 (1997-07-01)
4-Hydroxy-2-trans-nonenal, the most abundant and toxic unsaturated aldehyde generated during membrane lipid peroxidation, was synthesized starting from fumaraldehyde dimethyl acetal. In the first step of the synthesis, the fumaraldehyde dimethyl acetal was partially hydrolyzed using amberlyst catalyst to obtain the
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