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6-Carboxyfluorescein

HCID 76806
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Grundinformationen

CAS
3301-79-9
Standard-SMILES
O=C(O)c1ccc2c(c1)C1(OC2=O)c2ccc(O)cc2Oc2cc(O)ccc21
InChIKey
BZTDTCNHAFUJOG-UHFFFAOYSA-N
Summenformel
C21H12O7
Durchschnittliche Molmasse
376,32 g/mol
Monoisotopische Masse
376,05830272

Namen und Bezeichner

Bevorzugter Name
6-Carboxyfluorescein
Englischer Name
6-Carboxyfluorescein
Summenformel
C21H12O7
Molmasse
376.32

Namen und Synonyme

6-FAMCarboxyfluorescein3',6'-dihydroxy-3-oxo-3H-spiro[2-benzofuran-1,9'-xanthene]-6-carboxylic acid3',6'-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-6-carboxylic acid6-FAM Acid6-FAM, 6-CF6-FAM, FLUOS6-FAM (Green)6-Carboxyfluoroscein6-CARBOXYFLUORESCEIN

Datenbank-Bezeichner

CAS
3301-79-9
PubChem CID
76806
DTXSID
DTXSID6062965
ChEMBL
CHEMBL1614944、CHEMBL318164
ChEBI
CHEBI:39073
UNII
JHJ853P6SM
EC Number
636-503-2
Nikkaji
J277.784C

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
300 °C · >300 °C(lit.)
Siedepunkt
736.4 · 736.4±60.0 °C(Predicted)
Dichte
1.73 · 1.73±0.1 g/cm3(Predicted)
storage temp.
2 · Sealed in dry,2-8°C
Löslichkeit
DMSO: soluble
pka
3.3 · 3.3, 4.6, 6.4, 7.0(at 25℃)
Aggregatzustand
Solid
Farbe
Yellow to orange
BRN
54341 · 54341
Major Application
5 and · Diagnosis of hematologic cancer, nongastric diseases, detection of genetically modified wheat, chromosomes, gene expression, nucleic acid, hepatitis A virus, avian influenza virus subtype H5 and H5N1, SARS virus, herpex simplex virus
InChI
1S/C21H12O7/c22-11-2-5-14-17(8-11)27-18-9-12(23)3-6-15(18)21(14)16-7-10(19(24)25)1-4-13(16)20(26)28-21/h1-9,22-23H,(H,24,25)
InChIKey
BZTDTCNHAFUJOG-UHFFFAOYSA-N
SMILES
OC(=O)c1ccc2C(=O)OC3(c4ccc(O)cc4Oc5cc(O)ccc35)c2c1
CAS Datenbank
3301 · 3301-79-9(CAS DataBase Reference)
EPA chemische Informationen
-1 · Spiro[isobenzofuran-1(3H),9'-[9H]xanthene]-6-carboxylic acid, 3',6'-dihydroxy-3-oxo- (3301-79-9)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

F
10-21
wgk
3
tsca
TSCA listed
hs_code
3204 90 00
risk_code
36/37/38
hazard_code
Xi
safety_code
26-36/37
Speicherklasse
11 - Combustible Solids

Chemie und Industrie

Anwendungen · 1 Eintrag

Verwenden6-Carboxyfluorescein (6-FAM) is derivative of fluorescein giving stable derivative upon conjugation with biopolymers.It has been used to check the plasma membrane integrity in sperm cells. The single isomer, 6-FAM, contains a carboxylic acid that can be used to react with primary amines via carbodiimide activation of the carboxylic acid. Commercially available FAM is a mixture of two isomers, 5-FAM and 6-FAM, and the correct name is 5(6)-carboxyfluorescein.

Darstellung · 1 Eintrag

synthetische1,2,4-Benzenetricarboxylic anhydride (also called 4- carboxyphthalic anhydride, 25.0 g, 0.13 mol) was added to a solution of 1,3-dihydroxybenzene (also called resorcinol, 28.6 g, 0.26 mol) in methane sulfonic acid (1M). An air condenser was attached to the flask and the reaction was heated at 85 oC in an open vessel for 24 h. After cooling to room temperature, the reaction mixture was poured into 7 volumes of ice/water. An orange-yellow precipitate formed; this was collected by filtration and dried in an oven at 200 oC. This residue was recrystallized two times from methanol/hexane to give 1.0 g of 6- carboxyfluorescein methanesulfonic acid adduct preferentially crystallizes from MeOH/hexanes. The mother liquors from this procedure were collected, the solvent was removed in vacuo, and the residues were recrystallized two times from ethanol/hexanes to give 3.2 g of 5-carboxyfluorescein methanesulfonic acid adduct preferentially crystallizes from EtOH/hexanes. Finally, the mother liquors from this experiment were combined, evaporated to dryness, and recrystallized two times from methanol/hexanes to give another 3.0 g of 6-carboxyfluorescein methanesulfonic acid adduct preferentially crystallizes from MeOH/hexanes, making a total yield of 4.0 g, 40 %. Careful dropwise addition of conc. HCl(aq) to solutions of these methanesulfonic esters preferentially crystallizes from EtOH/hexanes and preferentially crystallizes from MeOH/hexanes in 4M sodium hydroxide gave 5-carboxyfluorescein and 6-carboxyfluorescein, respectively in near quantitative yield.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

5-Carboxyfluorescein

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Benzol-1,2,4-tricarbonsure-1,2-anhydrid

Nachgelagerte Produkte

6-Carboxyfluorescein N-succinimidyl ester

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Ergänzende Hinweise

DefinitionChEBI: 6-carboxyfluorescein is a monocarboxylic acid. It derives from a fluorescein (lactone form).