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704814

Sigma-Aldrich

1,4-Dioxane solution

NMR reference standard, 10 mM in D2O ("100%", 99.96 atom % D), NMR tube size 5 mm × 7 in.

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Empirical Formula (Hill Notation):
C4H8O2
CAS Number:
123-91-1
Molecular Weight:
88.11
EC Number:
232-148-9
MDL number:
MFCD00006571
PubChem Substance ID:
329762481
NACRES:
NA.12

grade

NMR reference standard

Quality Level

200

form

solution

concentration

10 mM in D2O ("100%", 99.96 atom % D)

technique(s)

NMR: suitable

NMR tube size

5 mm × 7 in.

SMILES string

C1COCCO1

InChI

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

InChI key

RYHBNJHYFVUHQT-UHFFFAOYSA-N

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This Item
611905612073684228
1,4-Dioxane solution NMR reference standard, 10 mM in D2O ("100%", 99.96 atom % D), NMR tube size 5 mm × 7 in.

Sigma-Aldrich

704814

1,4-Dioxane solution

1,4-Dioxane solution NMR reference standard, 40% in benzene-d6 (99.6 atom % D), chromium(III) acetylacetonate 5 mg/mL, NMR tube size 5 mm × 8 in.

Sigma-Aldrich

611905

1,4-Dioxane solution

1,4-Dioxane solution NMR reference standard, 40% in benzene-d6 (99.6 atom % D), chromium(III) acetylacetonate 5 mg/mL, NMR tube size 3 mm × 8 in.

Sigma-Aldrich

612073

1,4-Dioxane solution

1,4-Dioxane solution NMR reference standard, 40% in benzene-d6 (99.6 atom % D), NMR tube size 10 mm × 8 in.

Sigma-Aldrich

684228

1,4-Dioxane solution

form

solution

form

-

form

-

form

rod

concentration

10 mM in D2O ("100%", 99.96 atom % D)

concentration

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

concentration

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

concentration

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

technique(s)

NMR: suitable

technique(s)

NMR: suitable

technique(s)

NMR: suitable

technique(s)

NMR: suitable

NMR tube size

5 mm × 7 in.

NMR tube size

5 mm × 8 in.

NMR tube size

3 mm × 8 in.

NMR tube size

10 mm × 8 in.

Features and Benefits

13C sensitivity

Quantity

5 mm O.D. tube contains 0.700 mL.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Carlos E Agudelo-Morales et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 13(18), 4195-4201 (2012-10-24)
The quenching of pyrene and 1-methylpyrene fluorescence by nitroanilines (NAs), such as 2-, 3-, and 4-nitroaniline (2-NA, 3-NA, and 4-NA, respectively), 4-methyl-3-nitroaniline (4-M-3-NA), 2-methyl-4-nitroaniline (2-M-4-NA), and 4-methyl-3,5-dinitroaniline (4-M-3,5-DNA), are studied in toluene and 1,4-dioxane. Steady-state fluorescence data show the higher
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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
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