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luminol - 98%, high purity , CAS No.521-31-3

152 Citations COA COA
In stock
Item Number
L105655
Grouped product items
SKU Size
Availability
 Price Qty
L105655-1g
1g
2
$19.90
L105655-5g
5g
3
$49.90
L105655-25g
25g
3
$173.90
L105655-100g
100g
2
$486.90
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View related series
Chemiluminescence Reagent (3) Fluorescence/luminescent spectroscopic reagents (3) Fluorescent Dye (372) oxidative stress (41) Phthalazines (3) Six-Membered Heterocyclic Compounds (1696)

Basic Description

Synonyms 3-Aminophthalhydrazide | 5-Amino-2,3-dihydro-1,4-phthalazinedione | 5-amino-2,3-dihydrophthalazine-1,4-dione | 3-Aminophthalic hydrazide | 5-Amino-1,2,3,4-tetrahydrophthalazine-1,4-dione
Specifications & Purity Moligand™, ≥98%
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Product Description

Luminol is a reagent for the generation of chemiluminescence in biological assays including nitric oxide and myeloperoxidase assay. Luminol is converted to a dianion in basic solution, which is then oxidized with H2O2/Cu2+ to form N2 and an aminophthalate ion in an electronically excited state. The aminophthalate ion emits a photon of wavelength 424 nm.
A chemiluminescence generating reagent for biological and metal cation assays

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Diazanaphthalenes
Subclass Benzodiazines
Intermediate Tree Nodes Phthalazines
Direct Parent Phthalazinones
Alternative Parents Pyridazinones  Benzenoids  Vinylogous amides  Heteroaromatic compounds  Lactams  Azacyclic compounds  Primary amines  Organopnictogen compounds  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Phthalazinone - Pyridazinone - Pyridazine - Benzenoid - Heteroaromatic compound - Vinylogous amide - Lactam - Azacycle - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary amine - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as phthalazinones. These are compounds containing a phthalazine bearing a ketone group.
External Descriptors Not available

Associated Targets(Human)

TNF Tclin TNF-alpha (1897 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RAN Tchem GTP-binding nuclear protein Ran/Importin subunit beta-1/Snurportin-1 (21853 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Qtrt1 tRNA-guanine transglycosylase (21 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 5-amino-2,3-dihydrophthalazine-1,4-dione
INCHI InChI=1S/C8H7N3O2/c9-5-3-1-2-4-6(5)8(13)11-10-7(4)12/h1-3H,9H2,(H,10,12)(H,11,13)
InChIKey HWYHZTIRURJOHG-UHFFFAOYSA-N
Smiles C1=CC2=C(C(=C1)N)C(=O)NNC2=O
Isomeric SMILES C1=CC2=C(C(=C1)N)C(=O)NNC2=O
WGK Germany 3
RTECS TH8890060
Molecular Weight 177.16
Beilstein 383929
Reaxy-Rn 383929
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=383929&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

34 results found

Lot Number Certificate Type Date Item
F2512324 Certificate of Analysis May 30, 2025 L105655
F2512325 Certificate of Analysis May 30, 2025 L105655
F2512326 Certificate of Analysis May 30, 2025 L105655
F2512327 Certificate of Analysis May 30, 2025 L105655
B2528480 Certificate of Analysis Dec 19, 2024 L105655
B2528485 Certificate of Analysis Dec 19, 2024 L105655
B2528486 Certificate of Analysis Dec 19, 2024 L105655
K2415400 Certificate of Analysis Nov 05, 2024 L105655
K2415401 Certificate of Analysis Nov 05, 2024 L105655
K2415402 Certificate of Analysis Nov 05, 2024 L105655
K2415403 Certificate of Analysis Nov 05, 2024 L105655
H2407061 Certificate of Analysis Jun 26, 2024 L105655
G2411632 Certificate of Analysis Jun 26, 2024 L105655
G2411636 Certificate of Analysis Jun 26, 2024 L105655
G2411631 Certificate of Analysis Jun 26, 2024 L105655
G2411633 Certificate of Analysis Jun 26, 2024 L105655
G2411634 Certificate of Analysis Jun 26, 2024 L105655
G2411635 Certificate of Analysis Jun 26, 2024 L105655
F2426281 Certificate of Analysis Jun 14, 2024 L105655
D2422226 Certificate of Analysis Mar 11, 2024 L105655
D2422227 Certificate of Analysis Mar 11, 2024 L105655
C2414632 Certificate of Analysis Feb 29, 2024 L105655
L22071263 Certificate of Analysis Dec 15, 2022 L105655
D2306524 Certificate of Analysis Nov 22, 2022 L105655
D2306585 Certificate of Analysis Nov 22, 2022 L105655
D2306584 Certificate of Analysis Nov 22, 2022 L105655
D2306586 Certificate of Analysis Nov 22, 2022 L105655
I2216435 Certificate of Analysis Jul 28, 2022 L105655
I2216436 Certificate of Analysis Jul 28, 2022 L105655
I2216458 Certificate of Analysis Jul 28, 2022 L105655
I2216283 Certificate of Analysis Jul 28, 2022 L105655
K2302070 Certificate of Analysis Jul 28, 2022 L105655
H1815012 Certificate of Analysis Jun 18, 2022 L105655
G2221220 Certificate of Analysis Jun 18, 2022 L105655

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Chemical and Physical Properties

Solubility Soluble in DMSO (50 mg/ml), and 10% hot ammonia (100 mg/ml). Insoluble in water.
Sensitivity Air Sensitive
Melt Point(°C) ≥300°C
Molecular Weight 177.160 g/mol
XLogP3 0.300
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 0
Exact Mass 177.054 Da
Monoisotopic Mass 177.054 Da
Topological Polar Surface Area 84.200 Ų
Heavy Atom Count 13
Formal Charge 0
Complexity 254.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Alternative Products

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