47676
二甲醇缩甲醛
absolute, over molecular sieve (H2O ≤0.01%), ≥99.0% (GC)
别名:
二甲氧基甲烷, 甲缩醛
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线性分子式:
CH2(OCH3)2
化学文摘社编号:
分子量:
76.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-714-2
Beilstein/REAXYS Number:
1697025
MDL number:
Assay:
≥99.0% (GC)
InChI key
NKDDWNXOKDWJAK-UHFFFAOYSA-N
InChI
1S/C3H8O2/c1-4-3-5-2/h3H2,1-2H3
SMILES string
COCOC
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.)
functional group
acetal, ether
Quality Level
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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).
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-0.4 °F - closed cup
flash_point_c
-18 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
法规信息
危险化学品
此项目有
Calceolariaceae: floral development and systematic implications.
Mayr EM and Weber A.
American Journal of Botany, 93(3), 327-343 (2006)
Purification and dehydration of methylal by pervaporation.
Carretier E, et al.
Journal of Membrane Science , 217(1), 159-171 (2003)
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)
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)
Electrosynthesis of trimethylorthoformate on BDD electrodes.
Fardel R, et al.
J. Appl. Electrochem., 36(2), 249-253 (2006)
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