Chemodex

Luminol monosodium salt

CHF 183.00
In stock
CDX-L0014-G0055 gCHF 183.00
CDX-L0014-G02525 gCHF 732.00
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Product Details
Synonyms 3-Aminophthalhydrazide; 5-Amino-2,3-dihydro-1,4-phthal-azinedione
Product Type Chemical
Properties
Formula C8H6N3O2Na
MW 199.14
CAS 20666-12-0
Source/Host Chemicals Synthetic.
Purity Chemicals ≥98% (HPLC)
Appearance White to light yellow powder.
Solubility Soluble in water (50mg/ml).
Identity Determined by 1H-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 RVJVDCVIJCBUTH-UHFFFAOYSA-M
Smiles NC1=C2C(C(N([Na])NC2=O)=O)=CC=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°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.
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Product Specification Sheet
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Description

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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