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{{chembox {{chembox
| Watchedfields = changed
| verifiedrevid = 385697486 | verifiedrevid = 428136922
|Reference=<ref> at ]</ref> | Reference =<ref> at ]</ref>
|ImageFile= Fluorescamine.png | ImageFile = Fluorescamine.png
|ImageSize=200px | ImageSize =
|IUPACName=4'-phenylspiro-1,3'-dione | IUPACName =4'-phenylspiro-1,3'-dione
|OtherNames=Fluram | OtherNames =Fluram
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo=38183-12-9 | CASNo =38183-12-9
| PubChem=37927
| UNII_Ref = {{fdacite|correct|FDA}}
| SMILES=C1=CC=C(C=C1)C2=COC3(C2=O)C4=CC=CC=C4C(=O)O3
| UNII = Y6859V58YW
| PubChem =37927
| SMILES =C1=CC=C(C=C1)C2=COC3(C2=O)C4=CC=CC=C4C(=O)O3
| InChI = 1S/C17H10O4/c18-15-13(11-6-2-1-3-7-11)10-20-17(15)14-9-5-4-8-12(14)16(19)21-17/h1-10H
| InChIKey = ZFKJVJIDPQDDFY-UHFFFAOYSA-N
| MeSHName = D005450
| ChemSpiderID = 34768
}} }}
|Section2={{Chembox Properties |Section2={{Chembox Properties
| Formula=C<sub>17</sub>H<sub>10</sub>O<sub>4</sub> | Formula =C<sub>17</sub>H<sub>10</sub>O<sub>4</sub>
| MolarMass=278.26 g/mol | MolarMass =278.26 g/mol
| Appearance= | Appearance =
| Density= | Density =
| MeltingPt=153-157 °C | MeltingPtC = 153 to 157
| MeltingPt_notes =
| BoilingPt=
| BoilingPt =
| Solubility=
| Solubility =
}} }}
|Section3={{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards =
| FlashPt= | FlashPt =
| AutoignitionPt =
| Autoignition=
}} }}
}} }}


'''Fluorescamine''' is a ] that is not fluorescent itself, but reacts with primary amines to form highly fluorescent products. It hence has been used as a reagent for the detection of ]s and ]s. 1-100µg of protein and down 10pg protein can be detected<ref>Böhlen P. , S. Stein,W. Dairman, and S. Undenfriend, Arch. Biochem. Biophys. 155, 1973, 213–220</ref> <ref>] ]</ref>. This method is found to suffer of high blanks resulting of high rate of hydrolysis due to used excess concentration. Alternative methods are based on ], ] and ]. '''Fluorescamine''' is a ] that is not fluorescent itself, but reacts with primary amines to form highly fluorescent products, i.e. it is ]. It hence has been used as a reagent for the detection of ]s and ]s.<ref>{{cite journal |doi=10.1016/S0021-9673(00)82285-2 |title=Cactus alkaloids : XL. Identification of mescaline and other β-phenethylamines in ''Pereskia'', ''Pereskiopsis'' and ''Islaya'' by use of fluorescamine conjugates |journal=Journal of Chromatography A |volume=189 |pages=79–85 |year=1980 |last1=Doetsch |first1=Paul W. |last2=Cassady |first2=John M. |last3=McLaughlin |first3=Jerry L. }}</ref> 1-100&nbsp;μg of protein and down to 10 pg of protein can be detected.<ref>{{cite journal |doi=10.1016/S0003-9861(73)80023-2 |pmid=4736505 |title=Fluorometric assay of proteins in the nanogram range |journal=Archives of Biochemistry and Biophysics |volume=155 |issue=1 |pages=213–220 |year=1973 |last1=Böhlen |first1=Peter |last2=Stein |first2=Stanley |last3=Dairman |first3=Wallace |last4=Udenfriend |first4=Sidney }}</ref><ref>{{dead link|date=February 2019}} by ] </ref> Once bound to protein the excitation wavelength is 381 nm (near ultraviolet) and the emission wavelength is 470 nm (blue).<ref>{{cite web |last1=Biotium |title=Fluorescamine PRODUCT AND SAFETY DATA SHEET |url=https://biotium.com/wp-content/uploads/2017/10/PI-90092.pdf |publisher=Biotium |access-date=21 February 2023}}</ref> This method is found to suffer from high blanks resulting from a high rate of hydrolysis due to requiring a large excess concentration.<ref></ref> Alternative methods are based on ] (OPA), ] (DTNB), or ].

==Reaction==
:]{{clear-left}}

==See also==
* ]


==References== ==References==
{{reflist}} {{reflist}}

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