5-Aminofluorescein

Chemodex
Product Code: CDX-A0018
Supplier: Chemodex
CodeSizePrice
CDX-A0018-M250250 mg£50.00
Quantity:
CDX-A0018-G0011 g£109.00
Quantity:
CDX-A0018-G01010 g£617.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4 °C

Images

1 / 1
Chemical Structure

Chemical Structure

Further Information

Appearance:
Beige to brown solid.
CAS:
3326-34-9
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Protect from light and moisture.
Hazards:
H315, H319, H335
InChi:
InChI=1S/C20H13NO5/c21-10-1-4-14-13(7-10)19(24)26-20(14)15-5-2-11(22)8-17(15)25-18-9-12(23)3-6-16(18)20/h1-9,22-23H,21H2
InChiKey:
GZAJOEGTZDUSKS-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 3326-34-9. Formula: C20H13NO5. MW: 347.32. Synthetic. The uronic acid residues of all known glycosaminoglycuronans react wit 5-aminofluorescein to yield fluorescent derivatives, which show fluorescence characteristics identical to those of 5-acetamidofluorescein (CDX-A0089). 5-aminofluorescein is also used to prepare FITC Isomer I (CDX-F0011, CDX-F0020).
MDL:
MFCD00005052
Molecular Formula:
C20H13NO5
Molecular Weight:
347.32
Package Type:
Vial
Precautions:
P261, P305, P351, P338
Product Description:
The uronic acid residues of all known glycosaminoglycuronans react wit 5-aminofluorescein to yield fluorescent derivatives, which show fluorescence characteristics identical to those of 5-acetamidofluorescein (CDX-A0089). 5-aminofluorescein is also used to prepare FITC Isomer I (CDX-F0011, CDX-F0020).
Purity:
>95% (HPLC); 6-Isomer >1%
Signal word:
Warning
SMILES:
NC1=CC=C2C(=C1)C(=O)OC21C2=CC=C(O)C=C2OC2=CC(O)=CC=C12
Solubility Chemicals:
Soluble in acetone or methanol.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at +4°C.

References

(1) O.N. Burchak et al.; Bioorg. & Med. Chem. 14(8), 2559 (2006) | (2) H. Sigmund et al.; Helv. Chim. Acta, 86(7), 2299 (2003) | (3) A. Ogamo et al.; Carboh. Res. 105(1), 69 (1982)

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