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Merck
CN

611905

1,4-Dioxane solution

suitable for NMR (reference standard), 40% in benzene-d6 (99.6 atom % D), chromium(III) acetylacetonate 5 mg/mL, 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:
12352005
PubChem Substance ID:
24882077
NACRES:
NA.12

Key Documents

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composition

chromium(III) acetylacetonate, 5 mg/mL

Quality Level

200

concentration

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

technique(s)

NMR: suitable

NMR tube size

5 mm × 8 in.

suitability

suitable for NMR (reference standard)

SMILES string

C1COCCO1

InChI

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

InChI key

RYHBNJHYFVUHQT-UHFFFAOYSA-N

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Features and Benefits

13C sensitivity

Preparation Note

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)

70.0 °F - closed cup

Flash Point(C)

21.1 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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

Lot/Batch Number
EB1760
SZ1691
IY1769
CX0057
TV0272

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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
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
O N Makshakova et al.
Bioorganicheskaia khimiia, 38(3), 300-305 (2012-09-25)
Our interest in modifying influence of the low-molecular organic compounds on the hydration shell of biopolymers is due to a well-known fact that the former can act as regulators of the enzymatic activity changed the hydration shell of the latter.
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
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