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07985

6-Aminofluorescein

BioReagent, suitable for fluorescence, ~95% (HPLC)

Synonym(s):

Fluoresceinamine isomer II

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1 g
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$245.00
5 g
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$954.00
$477.00

About This Item

Empirical Formula (Hill Notation):
C20H13NO5
CAS Number:
51649-83-3
Molecular Weight:
347.32
NACRES:
NA.32
PubChem Substance ID:
329748535
UNSPSC Code:
12171500
EC Number:
257-334-7
MDL number:
MFCD00005051
Beilstein/REAXYS Number:
51708

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product line

BioReagent

Quality Level

100

assay

~95% (HPLC)

form

powder

impurities

≤5% 5-aminofluorescein

mp

285 °C (dec.) (lit.)

solubility

DMSO: soluble, acetone: soluble, methanol: soluble

fluorescence

λex 490 nm; λem 520 nm in 0.1 M Tris pH 9.0

suitability

suitable for fluorescence

SMILES string

Nc1ccc2C(=O)OC3(c4ccc(O)cc4Oc5cc(O)ccc35)c2c1

InChI

1S/C20H13NO5/c21-10-1-4-13-16(7-10)20(26-19(13)24)14-5-2-11(22)8-17(14)25-18-9-12(23)3-6-15(18)20/h1-9,22-23H,21H2

InChI key

YOAWSYSKQHLFPM-UHFFFAOYSA-N

Application

6-Aminofluorescein has been demonstrated to be useful fluorescent labeling reagent for fullerene-based liposome nanostructures termed ‘buckysomes′. 6-aminofluorescein dissolved in 0.1 N NaOH can be quantified from a maximum absorbance at 490 nm. Decarboxylated 6-aminofluorescein dissolved 6 N HCl (prepare by constant boiling at 110° C for 24 h) can be quantified from a maximum absorbance at 454 nm. Aldehyde groups are formed by oxidateive damage to proteins, which can be detected by conjugation to decarboxylated 6-aminofluorescein.

Other Notes

Note: Do not confuse with fluorescamine.

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This Item
20163434321-M408948
6-Aminofluorescein BioReagent, suitable for fluorescence, ~95% (HPLC)

Sigma-Aldrich

07985

6-Aminofluorescein

6-Aminofluorescein

Sigma-Aldrich

201634

6-Aminofluorescein

FITC, Isomer I

Sigma-Aldrich

34321-M

FITC, Isomer I

Isodecyl methacrylate 95%

Sigma-Aldrich

408948

Isodecyl methacrylate

suitability

suitable for fluorescence

suitability

-

suitability

-

suitability

-

fluorescence

λex 490 nm; λem 520 nm in 0.1 M Tris pH 9.0

fluorescence

-

fluorescence

-

fluorescence

-

solubility

DMSO: soluble, methanol: soluble, acetone: soluble

solubility

methanol: 1 mg/mL, clear, yellow to very dark yellow-orange

solubility

DMSO: 5 mg/mL, DMF: soluble, aqueous buffer, pH ≥ 9.0: soluble

solubility

-

form

powder

form

powder

form

solid

form

liquid

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

assay

~95% (HPLC)

assay

-

assay

≥95% (TLC)

assay

95%

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP1665
BCCL5900
BCCJ0074
BCCD8355
BCCC1277

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Articles

Sensor Dyes

Nitric oxide (NO) as a signal transporter in neurons, endothelial cells and in the immune system.

I Climent et al.
Analytical biochemistry, 182(2), 226-232 (1989-11-01)
Oxidative modification of proteins is implicated in a number of physiologic and pathologic processes. Metal-catalyzed oxidative modification usually causes inactivation of enzymes and the appearance of carbonyl groups in amino acid side chains of the protein. We describe use of
K C Ingham et al.
Biochimica et biophysica acta, 670(2), 181-189 (1981-09-29)
A method for covalent attachment of a fluorescent molecule to the carbohydrate moieties of glycoproteins is described. The glycoproteins were oxidized with periodate under mild conditions selective for sialic acid (Van Lenten, L. and Ashwell, G. (1971) J. Biol. Chem.
Miju Kim et al.
ACS nano, 9(8), 8269-8278 (2015-07-15)
Polyelectrolyte microcapsules represent versatile stimuli-responsive structures that enable the encapsulation, protection, and release of active agents. Their conventional preparation methods, however, tend to be time-consuming, yield low encapsulation efficiency, and seldom allow for the dual incorporation of hydrophilic and hydrophobic
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Global Trade Item Number

SKUGTIN
D193801-100G04061831835724
07985-5G04061832531328
07985-1G04061826660836