Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

Safety Information

06116

Sigma-Aldrich

6-(Iodoacetamido)fluorescein

suitable for fluorescence, ≥95% (HPLC)

Synonym(s):

6-IAF, N-(3′,6′-Dihydroxy-3-oxospiro[isobenzofuran-1(3H),9′-[9H]xanthen]-6-yl)-2-iodoacetamide

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C22H14INO6
CAS Number:
73264-12-7
Molecular Weight:
515.25
Beilstein:
13738833
MDL number:
MFCD00155654
UNSPSC Code:
12352200
PubChem Substance ID:
329748213
NACRES:
NA.32

Assay

≥95% (HPLC)

λmax

~489 nm in DMSO

fluorescence

λex 488 nm; λem 542 nm in DMF

suitability

suitable for fluorescence

storage temp.

2-8°C

SMILES string

Oc1ccc2c(Oc3cc(O)ccc3C24OC(=O)c5ccc(NC(=O)CI)cc45)c1

InChI

1S/C22H14INO6/c23-10-20(27)24-11-1-4-14-17(7-11)22(30-21(14)28)15-5-2-12(25)8-18(15)29-19-9-13(26)3-6-16(19)22/h1-9,25-26H,10H2,(H,24,27)

InChI key

YRDPEKZBFANDFE-UHFFFAOYSA-N

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

06116-25MG:4548173996943
06116-BULK:
06116-VAR:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Muhammad R Baig et al.
Journal of psychiatric practice, 16(5), 325-333 (2010-09-23)
There is increasing concern about the serious metabolic side effects and neurotoxicity caused by atypical (second-generation) antipsychotics. In a previous study by our group (Walss-Bass et al. Int J Neuropsychopharmacol 2008;11:1097-104), using a novel proteomic approach, we showed that clozapine
Hajo Haase et al.
Analytical biochemistry, 333(1), 19-26 (2004-09-08)
In the cellular environment, the sulfur ligands in zinc/thiolate coordination sites of proteins can be oxidized with concomitant mobilization of zinc. The characterization of such "redox zinc switches" requires the determination of three species, i.e., the zinc-containing complex and the
You Chen et al.
Journal of bacteriology, 191(13), 4392-4400 (2009-04-28)
The basic circadian oscillator of the unicellular fresh water cyanobacterium Synechococcus elongatus PCC 7942, the model organism for cyanobacterial circadian clocks, consists of only three protein components: KaiA, KaiB, and KaiC. These proteins, all of which are homomultimers, periodically interact
Chemical modifications of proteins as an aid to sequence analysis.
Alex F Carne
Methods in molecular biology (Clifton, N.J.), 211, 333-354 (2002-12-20)
Consuelo Walss-Bass et al.
The international journal of neuropsychopharmacology, 11(8), 1097-1104 (2008-05-10)
Although atypical antipsychotics are widely known to induce alterations in lipid and glucose metabolism, the mechanisms by which these alterations occur remain unknown. Several recent studies have shown that atypical antipsychotics induce oxidative stress and oxidative cell injury by increasing
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service