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
Beilstein/REAXYS Number:
1697039
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39021102
PubChem Substance ID:
NACRES:
NA.22
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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
SMILES string
COC(C)OC
InChI
1S/C4H10O2/c1-4(5-2)6-3/h4H,1-3H3
InChI key
SPEUIVXLLWOEMJ-UHFFFAOYSA-N
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General description
Kinetics of oxidative degradation of acetaldehyde dimethyl acetal has been studied by pulse radiolysis.[1] It also undergoes addition with various ketones, esters, amides and thioesters in the presence of silyl trifluoromethanesulfonates and an amine base.[2] 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.[3]
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk_germany
WGK 2
flash_point_f
1.4 °F - closed cup
flash_point_c
-17 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
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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)
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
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
G Catelani et al.
Carbohydrate research, 324(3), 204-209 (2000-03-21)
The reactivity order of O-deisopropylidenation of the three isopropylidene protecting groups of 2',6'-di-O-benzyl-2,3:5,6:3',4'-tri-O-isopropylidenelactose dimethyl acetal (2) with various reagents was established. The 5,6-acetal group was, although to a limited extent, more reactive as compared with the 3',4' group, while the
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