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Sigma-Aldrich

Formaldehyde dimethyl acetal

absolute, over molecular sieve (H2O ≤0.01%), ≥99.0% (GC)

Synonym(s):

Dimethoxymethane, Methylal

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About This Item

Linear Formula:
CH2(OCH3)2
CAS Number:
109-87-5
Molecular Weight:
76.09
Beilstein/REAXYS Number:
1697025
EC Number:
203-714-2
MDL number:
MFCD00008495
UNSPSC Code:
12352100
PubChem Substance ID:
57651079
NACRES:
NA.22

grade

absolute

assay

≥99.0% (GC)

quality

over molecular sieve (H2O ≤0.01%)

refractive index

n20/D 1.354

density

0.860 g/mL at 20 °C (lit.)

SMILES string

COCOC

InChI

1S/C3H8O2/c1-4-3-5-2/h3H2,1-2H3

InChI key

NKDDWNXOKDWJAK-UHFFFAOYSA-N

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General description

Formaldehyde dimethyl acetal (FDA, FDMA, FADMA, dimethoxymethane, DMM, methylal) is a biodegradable dimethyl acetal. It has been synthesized by condensing formaldehyde with methanol in the presence of acid catalyst. It is amphiphilic in nature with low viscosity, surface tension and boiling point. It is a flammable, highly volatile solvent with excellent dissolving power. It is reported to form trimethylorthoformate by anodic methoxylation in basic methanol.

Application

Formaldehyde dimethyl acetal may be used in the following studies:
  • Synthesis of methoxymethyl (MOM) ethers.
  • As an external cross-linker to form microporous polymers.
  • Dehydration of biological samples for scanning electron microscopy (SEM).

pictograms

Flame
GHS02

signalword

Danger

hcodes

H225

Hazard Classifications

Flam. Liq. 2

supp_hazards

EUH019

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

-0.4 °F - closed cup

flash_point_c

-18 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A new strategy to microporous polymers: knitting rigid aromatic building blocks by external cross-linker.
Li B, et al.
Macromolecules, 44(8), 2410-2414 (2011)
An efficient protocol for the preparation of MOM ethers and their deprotection using zirconium (IV) chloride.
Sharma GVM, et al.
Tetrahedron Letters, 45(50), 9229-9232 (2004)
Calceolariaceae: floral development and systematic implications.
Mayr EM and Weber A.
American Journal of Botany, 93(3), 327-343 (2006)
Jenn-Huei Lii et al.
Carbohydrate research, 340(5), 853-862 (2005-03-23)
The rotational barrier for a methyl group at the end of an anomeric system is sometimes lower than we might have anticipated. Thus, in the trans-trans conformation of dimethoxymethane, the barrier to methyl rotation is calculated (B3LYP/6-311++G(2d,2p)) to be 2.22
Electrosynthesis of trimethylorthoformate on BDD electrodes.
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