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Merck
CN

551368

1,4-Dioxane solution

suitable for NMR (reference standard), 40% in benzene-d6 (99.6 atom % D)

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About This Item

Empirical Formula (Hill Notation):
C4H8O2
CAS Number:
123-91-1
Molecular Weight:
88.11
NACRES:
NA.12
PubChem Substance ID:
24879218
UNSPSC Code:
12352005
MDL number:
MFCD00006571
Assay:
99% (CP)

Key Documents

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InChI

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

SMILES string

C1COCCO1

InChI key

RYHBNJHYFVUHQT-UHFFFAOYSA-N

assay

99% (CP)

concentration

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

technique(s)

NMR: suitable

NMR tube size

5 mm × 7 in. , 5 mm × 8 in.

suitability

suitable for NMR (reference standard)

Quality Level

200

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Features and Benefits

13C sensitivity

Preparation Note

5 mm O.D. tube contains 0.700 mL.

signalword

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

supp_hazards

EUH019

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

68.0 °F - closed cup

flash_point_c

20 °C - closed cup

ppe

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

Regulatory Information

危险化学品
美国出口管控产品
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Certificates of Analysis (COA)

Lot/Batch Number
MBBD2182
MBBC4786
MBBB6757V
MBBB3423V
EB0459

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Daniel Gerrity et al.
Water research, 46(19), 6257-6272 (2012-10-16)
The performance of ozonation in wastewater depends on water quality and the ability to form hydroxyl radicals (·OH) to meet disinfection or contaminant transformation objectives. Since there are no on-line methods to assess ozone and ·OH exposure in wastewater, many
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
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
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