Acetone-d6
Acetone-d6 structure
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Common Name | Acetone-d6 | ||
|---|---|---|---|---|
| CAS Number | 666-52-4 | Molecular Weight | 64.116 | |
| Density | 0.8±0.1 g/cm3 | Boiling Point | 46.5±3.0 °C at 760 mmHg | |
| Molecular Formula | C3D6O | Melting Point | -94ºC | |
| MSDS | Chinese USA | Flash Point | -17.2±0.0 °C | |
| Symbol |
GHS02, GHS07 |
Signal Word | Danger | |
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Determination of triacetone triperoxide using ultraviolet femtosecond multiphoton ionization time-of-flight mass spectrometry.
Anal. Chim. Acta 853 , 508-13, (2014) Triacetone triperoxide (TATP), an explosive compound, was measured using gas chromatography combined with multiphoton ionization time-of-flight mass spectrometry (GC/MPI-TOFMS). By decreasing the pulse width of a femtosecond laser from 80 to 35 fs, a molecula... |
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Characterization of diferuloylated pectic polysaccharides from quinoa (Chenopodium quinoa WILLD.).
Phytochemistry 116 , 320-8, (2015) In plants belonging to the order of Caryophyllales, pectic neutral side chains can be substituted with ferulic acid. The ability of ferulic acid to form intra- and/or intermolecular polysaccharide cross-links by dimerization was shown by the isolation and cha... |
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Differentiation of South American crack and domestic (US) crack cocaine via headspace-gas chromatography/mass spectrometry.
Drug Test. Anal. 7(3) , 241-6, (2015) South American 'crack' cocaine, produced directly from coca leaf, can be distinguished from US domestically produced crack on the basis of occluded solvent profiles. In addition, analysis of domestically produced crack indicates the solvents that were used fo... |
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Isoflavones with neuroprotective activities from fruits of Cudrania tricuspidata.
Phytochemistry 111 , 141-8, (2015) Ten isoflavones, cudraisoflavones B-K (1-10), together with 27 known isoflavones, were isolated from the EtOAc soluble extract of fruits of Cudrania tricuspidata. The structures of compounds 1-10 were elucidated on the basis of MS and NMR spectroscopic data, ... |
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Anionic derivatives of uracil: fragmentation and reactivity.
Phys. Chem. Chem. Phys. 16(33) , 17835-44, (2014) Uracil is an essential biomolecule for terrestrial life, yet its prebiotic formation mechanisms have proven elusive for decades. Meteorites have been shown to contain uracil and the interstellar abundance of aromatic species and nitrogen-containing molecules ... |
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Separation of derivatized glucoside anomers using supercritical fluid chromatography.
J. Chromatogr. A. 1418 , 218-23, (2015) Preparative scale supercritical fluid chromatography was used to separate derivatized anomeric monosaccharides. Methyl 2,3,4,6-tetra-O-benzoyl-α-d-glucopyranoside and methyl 2,3,4,6-tetra-O-benzoyl-β-d-glucopyranoside were synthesized by benzoyl derivatizatio... |
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Histone deacetylase inhibitor-polymer conjugate nanoparticles for acid-responsive drug delivery.
Eur. J. Med. Chem. 95 , 369-76, (2015) We report the synthesis of acid-responsive polymeric nanoparticles (NPs) consisting of a polymer-histone deacetylase inhibitor conjugate. An innovative aspect of this drug delivery particle lies in the NP conjugation of a histone deacetylase (HDAC) inhibitor,... |
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Non-transpeptidase binding arylthioether β-lactams active against Mycobacterium tuberculosis and Moraxella catarrhalis.
Bioorg. Med. Chem. 23(3) , 632-47, (2015) The prevalence of drug resistance in both clinical and community settings as a consequence of alterations of biosynthetic pathways, enzymes or cell wall architecture is a persistent threat to human health. We have designed, synthesized, and tested a novel cla... |
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Synthesis of (+)-crocacin D and simplified bioactive analogues.
Bioorg. Med. Chem. 23(5) , 1062-8, (2015) The total synthesis of (+)-crocacin D has been achieved in 15 steps (9 isolated intermediates) and 14% overall yield from commercially available starting materials and using (+)-crocacin C as a key intermediate. A number of simplified analogues and their biol... |
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Chitin dipentanoate as the new technologically usable biomaterial.
Mater. Sci. Eng. C. Mater. Biol. Appl. 55 , 50-60, (2015) In this article, the synthesis of novel biopolymer, chitin dipentanoate (Di-O-Valeryl Chitin, DVCH) has been described. DVCH is a chitin derivative esterified with two valeryl groups at positions 3 and 6 of the N-acetylglucosamine units and it is soluble in c... |