Diethylaminoethyl Methacrylate

C10H19NO2, 185.267 g/mol. Its structure, the values that were measured, the values that were calculated, and where each one came from.

Organic — ester5 measured properties

Drawn from the SMILES. It shows how the atoms are connected — not a photograph of a molecule, and not its shape in space.

Identifiers

Molecular formula: C₁₀H₁₉NO₂
Molecular weight: 185.267 g/mol
Exact mass: 185.141579 g/mol
SMILES: C=C(C)C(=O)OCCN(CC)CC
InChI: InChI=1S/C10H19NO2/c1-5-11(6-2)7-8-13-10(12)9(3)4/h3,5-8H2,1-2,4H3
InChIKey: SJIXRGNQPBQWMK-UHFFFAOYSA-N

Open in ReactionLens Use in reaction prediction

Both are open without an account.

Measured properties

Values somebody obtained from a sample and published. Where two sources report the same property they are both shown, in the units each used — a disagreement between them is information, and averaging it away would be inventing a number neither one gave.

Boiling Point: BP: 80 °C at 10 mm Hgmeasured · Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-174
Melting Point: -65.5 °C (freezing point)measured · BASF; N,N-Diethylaminoethyl Methacrylate (DEAEMA). Technical Information TI/CP 0007e, March 2012. Available from, as of Sept 4, 2015: https://www.specialty-monomers.basf.com/portal/streamer?fid=235727
Density: 0.92 g/cu cm at 20 °Cmeasured · Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-174
Vapor Pressure: 0.11 [mmHg]measured · reference compound database
Refractive Index: Index of refraction: 1.4442 at 20 °Cmeasured · Wilczynski R; Methacrylic Acid and Derivatives. Kirk-Othmer Encyclopedia of Chemical Technology. (1999-2015). New York, NY: John Wiley & Sons. Online Posting Date: March 14, 2003.

Calculated properties

Derived from the structure rather than from a sample. These are reproducible and they are not measurements: a calculated partition coefficient and a measured one can differ by a long way, and where both exist they are listed apart on purpose.

logP: 1.4475calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 29.54 Å²calculated · chemistry engine; Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors: 0calculated · chemistry engine; Atoms that can donate a hydrogen bond.
H-bond acceptors: 3calculated · chemistry engine; Atoms that can accept a hydrogen bond.
Rotatable bonds: 6calculated · chemistry engine; Single bonds the molecule can freely twist around.
Molar refractivity: 53.561 cm³/molcalculated · chemistry engine; Relates to the molecule's polarisability.
Fraction sp³ carbons: 0.7calculated · chemistry engine; Share of carbon atoms with tetrahedral bonding.
QED drug-likeness: 0.4631calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

C Carbon10 atoms · 64.8% by mass
O Oxygen2 atoms · 17.3% by mass
H Hydrogen19 atoms · 10.3% by mass
N Nitrogen1 atom · 7.6% by mass

Percentages are of the molecular weight above, worked out the same way the molar mass calculator does it.

Structure

Heavy atoms, hydrogen excluded: 13
Total atoms, hydrogen included: 32
Rings: 0
Aromatic rings: 0
Stereocentres: 0
Formal charge: 0

Functional groups

Ester
A carbonyl bonded to an oxygen that links to another carbon.
Ether
An oxygen bridging two carbons.
Tertiary amine
Nitrogen bonded to three carbons.
Alkene
A carbon–carbon double bond.

Matched by structural pattern, not by a measurement.

The molecule in three dimensions

Rotate and inspect the atoms. Loaded only when you ask, so the page stays light.

The drawing above is a diagram of what is bonded to what. A molecule is not flat, and the model here is one low-energy shape generated from the connectivity — useful for seeing which groups can reach each other, and not a measured structure. A real sample is a population of conformations, interconverting.

Reactions it appears in

No documented reaction with a written procedure and a source involves Diethylaminoethyl Methacrylate yet.

Other names for it

No systematic name is recorded.

The sources also call it 2-(Diethylamino)ethyl methacrylate, Daktose B, N,N-DIETHYLAMINOETHYL METHACRYLATE, 2-(diethylamino)ethyl 2-methylprop-2-enoate, 2-Propenoic acid, 2-methyl-, 2-(diethylamino)ethyl ester, 2-(N,N-Diethylamino)ethyl methacrylate, Methacrylic acid, 2-(diethylamino)ethyl ester, (2-(Methacryloyloxy)ethyl)diethylamine, ACRYESTER DE, AGEFLEX FM 2PTZ, DEAEM CPD, Et2NH-ethyl methacrylate.

Structurally related

Nothing structurally close to Diethylaminoethyl Methacrylate has a page here yet.

Where these values came from

chemistry engine
structure perception

No matching record was found in the currently indexed sources (reference compound database)..

What this page does not claim

The identifiers are what the source record holds, copied rather than recomputed. Measured values are reported as their source gave them, units and all; calculated values are marked as calculated and are not measurements. Where a field is absent the page says so, because a blank cell reads as a zero and a guessed value reads as a fact.

Nothing here is a hazard assessment, a purity statement or advice about handling a sample. A flash point quoted from a safety database is a number somebody published, not a judgement by us about whether this molecule is safe for what you intend.