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Trioxane

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Identification
Molecular formula
C6H12O3
CAS number
110-88-3
IUPAC name
2,4,6-trimethyl-1,3,5-trioxane
State
State

Trioxane is typically found as a solid at room temperature.

Melting point (Celsius)
61.50
Melting point (Kelvin)
334.65
Boiling point (Celsius)
115.00
Boiling point (Kelvin)
388.15
General information
Molecular weight
132.16g/mol
Molar mass
90.0780g/mol
Density
1.1730g/cm3
Appearence

Trioxane is a white, crystalline solid.

Comment on solubility

Solubility of 2,4,6-trimethyl-1,3,5-trioxane

2,4,6-trimethyl-1,3,5-trioxane, a cyclic organic compound, exhibits interesting solubility characteristics that are noteworthy:

  • Solvent Interaction: This compound is generally soluble in organic solvents such as ethanol, acetone, and ether.
  • Water Solubility: Interestingly, 2,4,6-trimethyl-1,3,5-trioxane has limited solubility in water due to its hydrophobic nature.
  • Temperature Dependence: The solubility may increase with rising temperatures in organic solvents, which can enhance molecular interactions.

It is significant to note that solubility is influenced by several factors, such as:

  • Polarity of Solvent: More polar solvents tend to dissolve more polar compounds, whereas 2,4,6-trimethyl-1,3,5-trioxane, being less polar, favors non-polar or moderately polar solvents.
  • Molecular Structure: The presence of multiple methyl groups contributes to its bulky structure, which further affects its solubility profile.

This summary encapsulates the solubility behavior of 2,4,6-trimethyl-1,3,5-trioxane, highlighting its compatibility with various solvents while illustrating the intricate relationship between molecular structure and solubility. In practical applications, understanding its solubility is essential for effective use in chemical formulations.

Interesting facts

Interesting Facts about 2,4,6-Trimethyl-1,3,5-Trioxane

2,4,6-trimethyl-1,3,5-trioxane is a fascinating compound notable for its unique structural makeup and applications. This compound, classified as a cyclic organic compound, features a trioxane ring, highlighting its innovative cyclic structure, which contributes to its intriguing reactivity and stability. Here are some engaging details:

  • Cyclic Ether: Being a trioxane, its structure consists of three oxygen atoms and two double-bonded carbon atoms in a ring formation, which is relatively rare among organic compounds.
  • Energy Density: This compound is recognized for its high energy density, making it a promising candidate in the field of fuel research and energy storage solutions.
  • Oxidative Stability: It demonstrates remarkable oxidative stability, which is an essential property for compounds used in various industrial applications, including as precursors in synthesis processes.
  • Application in Synthesis: Researchers often explore its potential in synthetic organic chemistry, especially as a building block for more complex molecules.
  • Polar Nature: The compound's polar nature opens up possibilities for interaction with different solvents, highlighting how polarity influences chemical behavior in reactions.

In conclusion, 2,4,6-trimethyl-1,3,5-trioxane is more than just a chemical formula; it represents a bridge between innovative chemistry and practical applications. Its unique properties in terms of stability and reactivity continue to intrigue scientists and professionals in the field.

Synonyms
PARALDEHYDE
2,4,6-Trimethyl-1,3,5-trioxane
123-63-7
Paracetaldehyde
Paral
Paraldehyd
Elaldehyde
Paraacetaldehyde
Triacetaldehyde
Paraldeide
p-Acetaldehyde
1,3,5-Trioxane, 2,4,6-trimethyl-
Acetaldehyde, trimer
1,3,5-Trimethyl-2,4,6-trioxane
2,4,6-Trimethyl-1,3,5-trioxacyclohexane
Paraldehyde Enema (BPC 1973)
Paraldehyde (USP)
Paraldehyde Draught (BPC 1973)
2,4,6-Trimethyl-1,3,5-trioxaan
2,4,6-Trimetil-1,3,5-triossano
DTXSID9023419
S6M3YBG8QA
NSC-9799
Paraldehyde [USP]
FEMA NO. 4010
CHEBI:27909
DTXCID003419
RefChem:858651
204-639-8
Acetaldehyde trimer
s-Trimethyltrioxymethylene
2,4,6-Trimethyl-s-trioxane
NSC 9799
RCRA waste number U182
Trimethyl trioxane
MFCD00036208
cis-2,4,6-Trimethyl-1,3,5-trioxane
Paral (TN)
s-Trioxane, 2,4,6-trimethyl-
2,4,6-Trimethyl-1,3,5-trioxan
1499-02-1
NCGC00159367-02
NCGC00159367-03
NCGC00159367-04
Paraldehyd [German]
Paraldehyde [USAN]
Paraldeide [Italian]
Triacetaldehyde [French]
CAS-123-63-7
HSDB 3375
EINECS 204-639-8
UNII-S6M3YBG8QA
UN1264
RCRA waste no. U182
BRN 0080142
Paraldehyde civ
AI3-03115
2,4,6-Trimethyl-1,3,5-trioxaan [Dutch]
DEA No. 2585
Paraldehyde; 2,4,6-Trimethyl-1,3,5-trioxane; cyclic trimer of acetaldehyde
2,4,6-Trimetil-1,3,5-triossano [Italian]
Aldehyde (para)
Paraldehyd(german)
Metaldehyde metabolite
s-Trimethyltrioxymethane
Paraldehyde, >=97%
Paraldehyde [UN1264] [Flammable liquid]
PARALDEHYDE [MI]
PARALDEHYDE [FHFI]
PARALDEHYDE [HSDB]
2,6-Trimethyl-s-trioxane
EC 204-639-8
PARALDEHYDE [VANDF]
PARALDEHYDE [MART.]
s-Trioxane,4,6-trimethyl-
SCHEMBL22870
PARALDEHYDE [WHO-DD]
5-19-09-00112 (Beilstein Handbook Reference)
CHEMBL1410743
SCHEMBL20072682
NSC9799
PARALDEHYDE CIV [USP-RS]
1,5-Trimethyl-2,4,6-trioxane
2,6-Trimethyl-1,3,5-trioxaan
2,6-Trimethyl-1,3,5-trioxane
2,6-Trimetil-1,3,5-triossano
DTXSID301271154
PARALDEHYDE [EP MONOGRAPH]
Paraldehyde, >=97.0% (GC)
PARALDEHYDE [USP MONOGRAPH]
Tox21_111607
Tox21_111608
Tox21_301299
1,5-Trioxane, 2,4,6-trimethyl-
BBL011471
STL146583
AKOS000120195
Tox21_111607_1
DB09117
UN 1264
WLN: T6O CO EOTJ B1 D1 F1
2,6-Trimethyl-1,3,5-trioxacyclohexane
NCGC00257534-01
VS-02956
NS00006360
P0019
Paraldehyde [UN1264] [Flammable liquid]
Paraldehyde, Lonza quality, >=99.5% (GC)
C07834
D00705
A805128
Q424342
F1908-0170
(2I+/-,4I+/-,6I+/-)-2,4,6-Trimethyl-1,3,5-trioxane
Paraldehyde, United States Pharmacopeia (USP) Reference Standard
InChI=1/C6H12O3/c1-4-7-5(2)9-6(3)8-4/h4-6H,1-3H