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Supelco

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

Empirical Formula (Hill Notation):
C4H8O2
CAS Number:
123-91-1
Molecular Weight:
88.11
MDL number:
MFCD00006571
UNSPSC Code:
12142201
PubChem Substance ID:
329765091
NACRES:
NA.24

grade

NMR reference standard
analytical standard

concentration

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

technique(s)

NMR: suitable

NMR tube size

5 mm × 8 in.

NMR tube wall thickness

0.24 mm , ultra-thin wall

format

single component solution

SMILES string

C1COCCO1

InChI

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

InChI key

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).

Features and Benefits

13C sensitivity

Quantity

5 mm O.D. tube contains 0.700 mL.

Signal Word

Danger

Hazard Classifications

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

Target Organs

Blood, Respiratory system

Supplementary Hazards

EUH019

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

53.6 °F - closed cup

Flash Point(C)

12 °C - closed cup

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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
Naoyuki Kishimoto et al.
Water research, 47(5), 1919-1927 (2013-02-09)
This paper reports on the reusability and the optimal reuse of iron-rich sludge for an electrochemical Fenton-type process using sequencing batch mode and separation batch mode reuse models. In the sequencing batch mode, processes of electrochemical treatment, neutralization, sedimentation, and
Sheau-Yun Dora Chiang et al.
Journal of environmental monitoring : JEM, 14(9), 2317-2326 (2012-07-25)
An intrinsic biodegradation study involving the design and implementation of innovative environmental diagnostic tools was conducted to evaluate whether monitored natural attenuation (MNA) could be considered as part of the remedial strategy to treat an aerobic aquifer contaminated with 1,4-dioxane
Megha Aggarwal et al.
PloS one, 7(12), e51288-e51288 (2012-12-20)
The nucleocapsid core interaction with endodomains of glycoproteins plays a critical role in the alphavirus life cycle that is essential to virus budding. Recent cryo-electron microscopy (cryo-EM) studies provide structural insights into key interactions between capsid protein (CP) and trans-membrane
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
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