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Home > Encyclopedia > Fluorescein 5-isothiocyanate

Fluorescein 5-isothiocyanate

Fluorescein 5-isothiocyanate structure

Fluorescein 5-isothiocyanate 

structure
  • CAS No:

    3326-32-7

  • Formula:

    C21H11NO5S

  • Chemical Name:

    Fluorescein 5-isothiocyanate

  • Synonyms:

    Spiro[isobenzofuran-1(3H),9′-[9H]xanthen]-3-one,3′,6′-dihydroxy-5-isothiocyanato-;Fluorescein,5-isothiocyanato-;3′,6′-Dihydroxy-5-isothiocyanatospiro[isobenzofuran-1(3H),9′-[9H]xanthen]-3-one;5-Isothiocyanatofluorescein;Fluorescein isothiocyanate isomer I;Fluorescein isothiocyanate isomer 1;Fluorescein 5-isothiocyanate;Fluoroscein-5-isothiocyanate;FITC isomer I;Fitc isomer 1;4-Isothiocyanatofluorescein;3′,6′-Dihydroxy-6-isothiocyanatospiro[2-benzofuran-3,9′-xanthene]-1-one;55177-69-0;86151-70-4;113394-21-1;122655-66-7;135680-00-1;1691330-05-8;1839547-28-2

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

FITC is a derivative of fluorescein for the labeling of amines.


Fluorescein 5-isothiocyanate is the 5-isomer of fluorescein isothiocyanate. Acts as a fluorescent probe capable of being conjugated to tissue and proteins; used as a label in fluorescent antibody staining procedures as well as protein- and amino acid-binding techniques.|Fluorescent probe capable of being conjugated to tissue and proteins. It is used as a label in fluorescent antibody staining procedures as well as protein- and amino acid-binding techniques.

Fluorescein 5-isothiocyanate Basic Attributes

389.381

389.38

222-042-0

I223NX31W9

29329990

Characteristics

120.44000

4.00

powder

1.5±0.1 g/cm3

>360 °C(lit.)

708.6±60.0 °C at 760 mmHg

382.4±32.9 °C

1.754

practically insoluble

2-8ºC

Safety Information

NONH for all modes of transport

3

R22;R36/37/38;R42/43

S22-S45-S36/37/39-S26-S36/37

Xn: Harmful;

Stability Stable, but moisture-sensitive. Incompatible with strong oxidizing agents, strong bases, amines, acids.

P261-P280-P342 + P311

H317-H334

|Danger|H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]|P261, P272, P280, P285, P302+P352, P304+P341, P321, P333+P313, P342+P311, P363, and P501|Aggregated GHS information provided by 167 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Chemicals that emit light after excitation by light. The wave length of the emitted light is usually longer than that of the incident light. Fluorochromes are substances that cause fluorescence in other substances, i.e., dyes used to mark or label other compounds with fluorescent tags. (See all compounds classified as Fluorescent Dyes.)

5 Isothiocyanatofluorescein

Fluorescein 5-isothiocyanate Use and Manufacturing

Uses

Fluorescein -5-isothiocyanate is a kind of fluorescent marker for biochemical applications. Reacts under mild conditions with primary amines and it is also used in modification of actin at lys-61, labelling of FAB and the modification of thiol groups. Fluorescent labeling reagent for proteins. Used in the fluorescent antibody technique for rapid identification of pathogens

Spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one, 3',6'-dihydroxy-5-isothiocyanato-: ACTIVE

Computed Properties

Molecular Weight:389.4
XLogP3:4.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:1
Exact Mass:389.03579362
Monoisotopic Mass:389.03579362
Topological Polar Surface Area:120
Heavy Atom Count:28
Complexity:668
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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