| Identification | Back Directory | [Name]
9-ANTHROYLNITRILE | [CAS]
85985-44-0 | [Synonyms]
9-ANTHROYLNITRILE
9-anthranoylnitrile
9-Anthracenecarbonyl cyanide
ANTHRACENE-9-CARBONYL CYANIDE
α-oxo-anthracene-9-acetonitrile
9-Anthraceneacetonitrile, α-oxo-
α-Oxo-anthracene-9-acetonitrile, 9-Anthroyl nitrile
3,3-diethyl-1-[(1-piperazinylamino)methyl]pyridine-2,4-dione | [Molecular Formula]
C16H9NO | [MDL Number]
MFCD00467599 | [MOL File]
85985-44-0.mol | [Molecular Weight]
231.25 |
| Chemical Properties | Back Directory | [Melting point ]
142-143 °C(lit.) | [Boiling point ]
426.8±14.0 °C(Predicted) | [density ]
1.266±0.06 g/cm3(Predicted) | [storage temp. ]
−20°C | [solubility ]
DMF: soluble | [form ]
solid | [color ]
Orange-yellow needles; Orange
powder | [λmax]
361 nm, 380 nm, 344 nm (MeOH | [BRN ]
8145431 | [Biological Applications]
Analyzing primary/secondary/tertiary alcohols; detecting aloesin,analytes, cortisol/cortisone in biological fluids,farnesyl pyrophosphate (FPP), archaeal ethercore lipids, thyroid hormones in pharmaceuticalpreparations, small quantities of triamcinolone(TMC); identifying serine 181; reagents forhydroxy steroids; separating/characterizing bileacid N-acetylglucosaminides; separating carnitineenantiomers in pharmaceuticals; reagents foralcohols/hydroxyl groups, | [Major Application]
Analyzing chemical
compositions for carbonized distillate of coal-tar refined
soft pitch; detecting absolute amount of resin-bound
hydroxyl groups | [InChI]
1S/C16H9NO/c17-10-15(18)16-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)16/h1-9H | [InChIKey]
FMKFDGUBVPIERQ-UHFFFAOYSA-N | [SMILES]
O=C(C#N)c1c2ccccc2cc3ccccc13 |
| Hazard Information | Back Directory | [Description]
9-Anthracenecarbonyl cyanide is a fluorescent probe used in the derivatization of glucocorticoids to aid their detection and separation using RP-HPLC with fluorescence detection. | [Uses]
9-Anthroyl nitrile is a fluorescent reagent useful in the derivatization of glucocorticoids to aid their detection and separation using RP-HPLC with fluorescence detection. It forms fluorescent esters by reacting with primary the hydroxyl group at the position 21 of the carbon chain on the glucocorticoid . | [Excitation / Emission Maximum]
360nm/460nm |
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