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Sigma-Aldrich

1,4-Dioxane-d8

≥99 atom % D

Synonyme(s) :

p-Dioxane-d8, Octadeuterodioxane

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About This Item

Formule empirique (notation de Hill):
C4D8O2
Numéro CAS:
Poids moléculaire :
96.15
Numéro Beilstein :
1307286
Numéro CE :
Numéro MDL:
Code UNSPSC :
12142201
ID de substance PubChem :
Nomenclature NACRES :
NA.21

Pureté isotopique

≥99 atom % D

Niveau de qualité

Pureté

≥99% (CP)

Forme

liquid

Technique(s)

NMR: suitable

Indice de réfraction

n20/D 1.4198 (lit.)

Point d'ébullition

99 °C (lit.)

Pf

12 °C (lit.)

Densité

1.129 g/mL at 25 °C (lit.)

Changement de masse

M+8

Chaîne SMILES 

[2H]C1([2H])OC([2H])([2H])C([2H])([2H])OC1([2H])[2H]

InChI

1S/C4H8O2/c1-2-6-4-3-5-1/h1-4H2/i1D2,2D2,3D2,4D2

Clé InChI

RYHBNJHYFVUHQT-SVYQBANQSA-N

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Description générale

1,4-Dioxane-d8 is a deuterated derivative of 1,4-dioxane. It has an isotopic purity of 99atom%D. It is a standard purity solvent suitable for routine NMR analyses (conducted at ambient temperatures where quality is less critical). It is widely employed as a deuterated standard. It participates as a surrogate standard during the activated carbon SPE (solid-phase extraction) and GC-MS-SIM (gas chromatography-mass spectrometry (GC-MS) in selected ion monitoring (SIM) mode) quantification of 1,4-dioxane in drinking water.

Application

  • Neutron Scattering of Residual Hydrogen in 1,4-Dioxane-d8 Liquid: Understanding Measurements with Molecular Dynamics Simulations: This study utilizes 1,4-Dioxane-d8 to enhance neutron scattering measurements, providing crucial data for researchers in material science and analytical chemistry on solvent behavior and molecular interactions (de Almeida et al., 2016).
  • Biodegradation of 1,4-dioxane and transformation of related cyclic compounds by a newly isolated Mycobacterium sp. PH-06: This research highlights the degradation pathways of 1,4-Dioxane-d8, contributing to environmental sciences by offering insights into bioremediation techniques that mitigate solvent impact (Kim et al., 2009).
  • Degradation of 1,4-dioxane and cyclic ethers by an isolated fungus: Explores the fungal degradation of cyclic ethers, including 1,4-Dioxane-d8, underscoring its significance in environmental cleanup and testing standards for academic and pharmaceutical research on organic pollutant breakdown (Nakamiya et al., 2005).

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Pictogrammes

FlameHealth hazardExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Organes cibles

Respiratory system

Risques supp

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

41.0 °F - closed cup

Point d'éclair (°C)

5 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificats d'analyse (COA)

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Les clients ont également consulté

Method development for the analysis of 1, 4-dioxane in drinking water using solid-phase extraction and gas chromatography-mass spectrometry
Grimmett PE and Munch JW.
Journal of Chromatographic Science, 47(1), 31-39 (2009)

Articles

Use this reference table to find the coupling values and chemical shifts of our NMR (deuterated) solvents. Melting and boiling points, molecular weight, density, and CAS number are also listed.

Use this reference table to find the coupling values and chemical shifts of our NMR (deuterated) solvents. Melting and boiling points, molecular weight, density, and CAS number are also listed.

Use this reference table to find the coupling values and chemical shifts of our NMR (deuterated) solvents. Melting and boiling points, molecular weight, density, and CAS number are also listed.

Use this reference table to find the coupling values and chemical shifts of our NMR (deuterated) solvents. Melting and boiling points, molecular weight, density, and CAS number are also listed.

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