CHEBI:85061 - N,N-dimethylformamide dimethyl acetal

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ChEBI Name N,N-dimethylformamide dimethyl acetal
ChEBI ID CHEBI:85061
ChEBI ASCII Name N,N-dimethylformamide dimethyl acetal
Definition An acetal obtained by formal condensation of N,N-dimethylformamide with methanol. N,N-dimethylformamide dimethyl acetal is a derivatisation agent used in gas-chromatography applications
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Philippe Rocca-Serra
Supplier Information
Download Molfile XML SDF
Formula C5H13NO2
Net Charge 0
Average Mass 119.16220
Monoisotopic Mass 119.09463
InChI InChI=1S/C5H13NO2/c1-6(2)5(7-3)8-4/h5H,1-4H3
InChIKey ZSXGLVDWWRXATF-UHFFFAOYSA-N
SMILES COC(OC)N(C)C
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Application(s): chromatographic reagent
A reagent used to improve selectivity in chromatographic analyses or separations, e.g. by formation of a derivative or by modification of the mobile phase.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N,N-dimethylformamide dimethyl acetal (CHEBI:85061) has functional parent N,N-dimethylformamide (CHEBI:17741)
N,N-dimethylformamide dimethyl acetal (CHEBI:85061) has role chromatographic reagent (CHEBI:59745)
N,N-dimethylformamide dimethyl acetal (CHEBI:85061) is a acetal (CHEBI:59769)
N,N-dimethylformamide dimethyl acetal (CHEBI:85061) is a tertiary amino compound (CHEBI:50996)
IUPAC Name
1,1-dimethoxy-N,N-dimethylmethanamine
Synonyms Sources
1,1-Dimethoxytrimethylamine ChemIDplus
Dimethoxy(dimethylamino)methane NIST Chemistry WebBook
dimethylformamide dimethyl acetal ChEBI
Dimethylformamide-dimethylacetal ChemIDplus
DMF Dimethyl acetal NIST Chemistry WebBook
DMF-DMA SUBMITTER
DMFDMA ChEBI
N-(Dimethoxymethyl)dimethylamin NIST Chemistry WebBook
Registry Numbers Types Sources
4637-24-5 CAS Registry Number NIST Chemistry WebBook
4637-24-5 CAS Registry Number ChemIDplus
506020 Reaxys Registry Number Reaxys
Last Modified
25 March 2015