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1,4-Dioxane solution

NMR reference standard, 40% in benzene-d6 (99.6 atom % D), NMR tube size 5 mm × 8 in.

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About This Item

Formule empirique (notation de Hill):
C4H8O2
Numéro CAS:
123-91-1
Poids moléculaire :
88.11
Numéro MDL:
MFCD00006571
Code UNSPSC :
12142201
ID de substance PubChem :
329765091
Nomenclature NACRES :
NA.24

Qualité

NMR reference standard
analytical standard

Niveau de qualité

200

Concentration

40% in benzene-d6 (99.6 atom % D)

Technique(s)

NMR: suitable

Taille du tube de RMN

5 mm × 8 in.

Épaisseur de la paroi du tube de RMN

0.24 mm , ultra-thin wall

Format

single component solution

Chaîne SMILES 

C1COCCO1

InChI

1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2

Clé InChI

RYHBNJHYFVUHQT-UHFFFAOYSA-N

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Application


  • Catalytic Oxidation of 1,4-Dioxane: Fe-ZSM-5 zeolite catalysts were investigated for the heterogeneous Fenton oxidation of 1,4-dioxane, evaluating the effects of Si/Al ratios and contributions of reactive oxygen species. This study highlights the use of 1,4-dioxane solutions in environmental remediation technologies, particularly in removing persistent organic pollutants from wastewater (Tian et al., 2024).

  • Groundwater Remediation: Research focused on the cometabolism of chlorinated volatile organic compounds and 1,4-dioxane in groundwater, employing 1,4-dioxane as a model compound to study the biodegradation processes and interactions with microbial communities. This study is crucial for developing effective strategies for groundwater treatment and ensuring the safety of pharmaceutical water sources (Clark & Rhea, 2023).

  • Structural Analysis of Hyaluronan: The study used a mixed solvent system including 1,4-dioxane for the structural analysis of hyaluronan oligosaccharides, forming double-helical duplexes. (Kolaříková et al., 2024).

Caractéristiques et avantages

13C sensitivity

Quantité

5 mm O.D. tube contains 0.700 mL.

Pictogrammes

FlameHealth hazardExclamation mark
GHS02,GHS08,GHS07

Mention d'avertissement

Danger

Classification des risques

Aquatic Chronic 3 - Asp. Tox. 1 - Carc. 1A - Eye Irrit. 2 - Flam. Liq. 2 - Muta. 1B - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

Organes cibles

Blood, Respiratory system

Risques supp

EUH019

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

53.6 °F - closed cup

Point d'éclair (°C)

12 °C - closed cup

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Iñaki Galve et al.
Molecular diversity, 16(4), 639-649 (2012-10-12)
A practical protocol was developed for the synthesis of 2-arylamino substituted 4-amino-5,6-dihydropyrido[2,3-d]pyrimidin-7(8H)-ones from α,β-unsaturated esters, malononitrile, and an aryl substituted guanidine via the corresponding 3-aryl-3,4,5,6- tetrahydropyrido[2,3-d]pyrimidin-7(8H)-ones. Such compounds are formed upon treatment of 2-methoxy-6-oxo-1,4,5,6-tetrahydropyridine-3-carbonitriles with an aryl substituted guanidine in
Kiyoaki Ishimoto et al.
Biomacromolecules, 13(11), 3757-3768 (2012-09-19)
For developing broader application of biobased polymers, graft copolymers and comb polymers having poly(lactic acid) (PLA) side chains have been synthesized by using a macromonomer technique. PLA macromonomers (MMm) having a methacryloyl polymerizable group with different PLA chain length with
R Dario Arrua et al.
Journal of chromatography. A, 1273, 26-33 (2013-01-01)
Rigid monolithic cryostructures were prepared in capillary format at sub-zero temperatures and used successfully in the separation of proteins by hydrophobic interaction chromatography (HIC). The polymerization mixture consisted of poly(ethyleneglycol) diacrylate (PEGDA) M(n)∼258 as the single monomer, a mixture of
B Thanuja et al.
Ultrasonics sonochemistry, 19(6), 1213-1220 (2012-04-14)
Density (ρ), ultrasonic velocity (U), for the binary mixtures of 4-methoxy benzoin (4MB) with ethanol, chloroform, acetonitrile, benzene, and di-oxane were measured at 298K. The solute-solvent interactions and the effect of the polarity of the solvent on the type of
Christof Aellig et al.
ChemSusChem, 5(9), 1737-1742 (2012-07-05)
The dehydration of D-fructose to 5-hydroxymethylfurfural was studied under single-phase conditions in the low boiling solvent 1,4-dioxane at moderate temperatures in the presence of the solid acid-catalyst Amberlyst-15. The reaction was first examined and optimized under batch conditions, where it
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