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D2938

Sigma-Aldrich

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

powder

Synonym(s):

4,5-Diaminofluorescein, DAF-2

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About This Item

Linear Formula:
C20H14N2O5 · 2C3H8O
CAS Number:
Molecular Weight:
482.53
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

Assay

≥98% (HPLC)

form

powder

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

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

InChI key

USEFIEWGHVUNEC-UHFFFAOYSA-N

Application

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

Formula variant

isopropanol adduct

Legal Information

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Kazuki Sato et al.
SpringerPlus, 3, 274-274 (2014-10-04)
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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
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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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