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2,6-dimethyl-4-tridecylmorpholine

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Identification
Molecular formula
C19H39NO
CAS number
63990-84-1
IUPAC name
2,6-dimethyl-4-tridecyl-morpholine
State
State

At room temperature, 2,6-dimethyl-4-tridecylmorpholine is in a liquid state. It exhibits low volatility and may produce a noticeable odor if not contained properly.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
323.30
Boiling point (Kelvin)
596.45
General information
Molecular weight
297.52g/mol
Molar mass
297.5190g/mol
Density
0.9325g/cm3
Appearence

2,6-dimethyl-4-tridecylmorpholine is generally a colorless oil-like liquid. It's slightly viscous in nature.

Comment on solubility

Solubility of 2,6-dimethyl-4-tridecyl-morpholine

The solubility of 2,6-dimethyl-4-tridecyl-morpholine can be influenced by several factors, including its molecular structure and the solvents used. This compound is part of the morpholine family, characterized by its unique nitrogen-containing ring structure, which can alter its solubility profile significantly.

Here are some key points to consider:

  • Polarity: Morpholines typically have moderate polarity, making them soluble in both polar and nonpolar solvents to a degree.
  • Chain Length: The long tridecyl chain (C13) in this compound tends to enhance lipophilicity, which can increase solubility in organic solvents.
  • Hydrogen Bonding: The ability of the morpholine nitrogen to engage in hydrogen bonding can improve solubility in polar solvents like water, although the long hydrophobic tail may counteract this effect.
  • Solvent Compatibility: Generally, it may dissolve well in organic solvents such as ethanol, hexane, and dichloromethane, while being less soluble in water.

In summary, the solubility of 2,6-dimethyl-4-tridecyl-morpholine is impacted by its complex structure, with interactions between its hydrophilic and hydrophobic portions determining its behavior in various solvents. As always, it's best to conduct experimental assessments for precise solubility data.

Interesting facts

Exploring 2,6-Dimethyl-4-tridecyl-morpholine

2,6-Dimethyl-4-tridecyl-morpholine is a fascinating compound that showcases the diversity of chemical structures and their implications in various fields. Here are some intriguing facts about this compound:

  • Morpholine Backbone: The compound features a morpholine ring, which is a heterocyclic structure containing both nitrogen and oxygen. This unique composition allows morpholines to exhibit diverse chemical properties and behaviors.
  • Applications in Industry: Morpholine derivatives, including 2,6-dimethyl-4-tridecyl-morpholine, find applications in several industries. They are often utilized as solvents, surfactants, and in the synthesis of pharmaceuticals and agrochemicals.
  • Octanol-Water Partition Coefficient: Compounds like this one can exhibit interesting partitioning behavior, which has implications for environmental chemistry, particularly in understanding the bioaccumulation and toxicity in aquatic systems.
  • Structure Activity Relationship (SAR): Understanding how varying the alkyl chain lengths and substitutions on the morpholine ring affects biological activity can guide the development of more effective compounds in medicinal chemistry.

As a scientist or chemistry student, exploring such compounds broadens our understanding of organic chemistry and its real-world applications. Investigating the relationships between molecular structure and physical properties continues to be a key area of research.

In the words of a renowned chemist, “The beauty of chemistry lies in its ability to combine different elemental characters into a single entity, revealing unexpected relationships and functionalities.”

Thus, 2,6-dimethyl-4-tridecyl-morpholine not only represents a specific chemical entity but also opens doors to further exploration in both academic and industrial scenarios.

Synonyms
Tridemorph
Calixin
Calixine
81412-43-3
Tridemorphe
Kalixin
F 220 (fungicide)
Tridemorf
BASF 220F
BAS 2203F
4-Tridecyl-2,6-dimethylmorpholine
N-Tridecyl-2,6-dimethylmorpholin
Elbamorph
Dimethyl-2,6 tridecyl-4 morpholine
0YZ4Z668EY
RefChem:933375
CALIXIN-86 OL
CHEBI:9700
BAS-2203F
DTXSID60893036
246-347-3
24602-86-6
2,6-DIMETHYL-4-TRIDECYLMORPHOLINE
Morpholine, 2,6-dimethyl-4-tridecyl-
Kalinin
N-Tridecyl-2,6-dimethylmorpholine
Tridemorph [ISO]
Tridemorph [BSI:ISO]
BAS 2205-F
Tridemorph (Mix of Isomers)
NSC 232676
DTXSID3041376
E-236
2,6-dimethyl-4-tridecyl-morpholine
Morpholine, 2,6-dimethyl-N-tridecyl-
Tridemorph (Technical Grade)
Tridemorf [Czech]
Caswell No. 386
Tridemorphe [ISO-French]
Tridemorph (technical)
EINECS 246-347-3
EPA Pesticide Chemical Code 121401
BRN 0608429
UNII-0YZ4Z668EY
N-Tridecyl-2,6-dimethylmorpholin [German]
UNII-784443KX6H
Dimethyl-2,6 tridecyl-4 morpholine [French]
Morpholine, 2,6-dimethyl-4-tridecyl-; 2,6-Dimethyl-4-tridecylmorpholine; N-Tridecyl-2,6-dimethylmorpholine; NSC 232676; Tridemorph
SCHEMBL28670
orb1739857
CHEMBL2286765
DTXCID1021376
CHEBI:83365
Morpholine,6-dimethyl-4-tridecyl-
2,6-dimethyl-n-tridecyl-morpholine
MSK21147
Tox21_300591
BDBM50487253
MFCD00055522
NSC232676
AKOS015914987
784443KX6H
NSC-232676
NCGC00248097-01
NCGC00254333-01
AC-19786
AS-76727
CAS-24602-86-6
DB-056525
NS00004563
Tridemorph, PESTANAL(R), analytical standard
(2Xi,6Xi)-2,6-dimethyl-4-tridecylmorpholine
G83041
A817389
A840125
Q209280