Luminol

CHF 153.00
In stock
CDX-L0012-G02525 gCHF 153.00
CDX-L0012-G100100 gCHF 459.00
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Product Details
Synonyms 3-Aminophthalhydrazide; 5-Amino-2,3-dihydro-1,4-phthalazinedione; NSC5064
Product Type Chemical
Properties
Formula C8H7N3O2
MW 177.16
CAS 521-31-3
RTECS TH8890060
Source/Host Chemicals Synthetic.
Purity Chemicals ≥97% (Titration)
Appearance White to light yellow powder.
Solubility Soluble in DMSO (50mg/ml). Insoluble in water.
Identity Determined by NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key HWYHZTIRURJOHG-UHFFFAOYSA-N
Smiles NC1=CC=CC2=C1C(=O)NNC2=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +4°C
Handling Advice Keep cool and dry.
Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
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Product Specification Sheet
Datasheet Download PDF

Very efficient and commonly used chemiluminiscent compound in many applications. Cyclic diacyl hydrazide that exhibits chemiluminescence upon oxidation. Oxidizing agents capable of initiating this particular reaction are nitrogen dioxide, PAN, hydrogen peroxide, ozone and other atmospheric oxidants. As an example, HRP combined with hydrogen peroxide as an activator, causes luminescent peroxidation of luminol. This reaction can be enhanced by certain phenol derivatives, such as p-substituted phenols. Luminol can also be oxidized and chemiluminesce, by compounds containing iron, copper, gold, and cyanide. Luminol is a reagent for the generation of chemiluminescence in biological assays including nitric oxide and myeloperoxidase assays or in fornensic blood tests. Spectral data: λex=355nm, λem=411nm.

Product References

(1) M.J. Cormier & P.M. Prichard; J. Biol. Chem. 243, 4706 (1968) | (2) G.H.G. Thorpe, et al.; Clin. Chem. 31, 1335 (1985) | (3) T.I. Quickenden & J.I. Creamer; Luminescence 16, 295 (2001) | (4) A. Fan, et al.; Anal. Sci. 25, 5877 (2009) | (5) Y.A. Vladimirov, et al.; Biochem. 74, 1545 (2009)

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