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D2938

Sigma-Aldrich

4,5-Diaminofluorescein-Isopropanol adduct (1:2)

powder

Synonyme(s) :

4,5-Diaminofluorescein, DAF-2

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About This Item

Formule linéaire :
C20H14N2O5 · 2C3H8O
Numéro CAS:
205391-01-1
Poids moléculaire :
482.53
Numéro MDL:
MFCD11045988
Code UNSPSC :
12171500
ID de substance PubChem :
329798761
Nomenclature NACRES :
NA.47

Pureté

≥98% (HPLC)

Forme

powder

Application(s)

diagnostic assay manufacturing
hematology
histology

Température de stockage

room temp

Chaîne SMILES 

CC(C)O.CC(C)O.Nc1cc2C(=O)OC3(c4ccc(O)cc4Oc5cc(O)ccc35)c2cc1N

InChI

1S/C20H14N2O5.2C3H8O/c21-15-7-11-14(8-16(15)22)20(27-19(11)25)12-3-1-9(23)5-17(12)26-18-6-10(24)2-4-13(18)20;2*1-3(2)4/h1-8,23-24H,21-22H2;2*3-4H,1-2H3

Clé InChI

USEFIEWGHVUNEC-UHFFFAOYSA-N

Application

Fluorescent detector of nitric oxide in culture medium, tissue sections and biopsy cells

Variante de formule

isopropanol adduct

Informations légales

DAF-2 is manufactured by Daiichi Pure Chemicals Co., LTD.
US Patent No. 5,874,590

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Kazuki Sato et al.
SpringerPlus, 3, 274-274 (2014-10-04)
The Gram-negative bacterium Photorhabdus luminescens which symbiotically associates with the entomopathogenic nematode Heterorhabditis bacteriophora, has a broad insecticidal and nematicidal activity. The virulence of P. luminescens toward the non-mutualistic nematode Caenorhabditis elegans has not been described. We showed that when
Isabella Echeverri et al.
American journal of human biology : the official journal of the Human Biology Council, 27(6), 822-831 (2015-05-07)
To evaluate the Relationship between maternal and newborn endothelial function and oxidative stress. Forty-three pregnant women and their offspring were evaluated. As markers of endothelial function, the flow-mediated dilation (FMD) was measured in pregnant women in the second and third
Jae Sue Choi et al.
Archives of pharmacal research, 37(10), 1354-1363 (2014-07-06)
To investigate the effect of C-glycosylation at different positions of luteolin, the structure-activity relationships of luteolin and a pair of isomeric C-glycosylated derivatives orientin and isoorientin, were evaluated. We investigated the effects of C-glycosylation on the antioxidant, anti-Alzheimer's disease (AD)
Marta Rogowska et al.
Natural product communications, 10(11), 1825-1828 (2016-01-12)
The aim of the study was to determine the scavenging capacity of aqueous and ethanolic extracts derived from the herb of two species of Galinsoga against NO and ONOO-. In both tests the aqueous extracts of both Galinsoga species were
Naira Poerner Rodrigues et al.
Journal of agricultural and food chemistry, 63(19), 4815-4826 (2015-04-25)
The influence of green coffee genotype on the bioactive compounds and the in vitro antioxidant capacity against the principal reactive oxygen (ROO(•), H2O2, HO(•), and HOCl) and nitrogen (NO(•) and ONOO(-)) species of biological relevance was investigated. This is the
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