JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Small Molecules & Compound Libraries
Signaling Pathways
NF-κB
Reactive Oxygen Species
Phthalazine - >98.0%, high purity , CAS No.253-52-1

Skip to the end of the images gallery

Skip to the beginning of the images gallery

Phthalazine - >98.0%, high purity , CAS No.253-52-1

1 Citations

COA

Grade & Purity:

≥98%

Cas Number: 253-52-1
Molecular Weight: 130.15
Beilstein Registry Number: 23174
MDL number: MFCD00006908
PubChem CID: 9207
PubChem SID: 488180941

In stock

Item Number

P160145

Grouped product items
SKU	Size	Availability	Price
P160145-1g	1g	3	$9.90
P160145-5g	5g	4	$25.90
P160145-10g	10g	2	$46.90
P160145-25g	25g	4	$77.90
P160145-100g	100g	2	$280.90

View related series

Glucose Metabolism (1943) pyridazines (58) Six-Membered Heterocyclic Compounds (1696)

Basic Description

Synonyms	PHTHALAZINE [USP IMPURITY] \| Q6593919 \| CCRIS 6894 \| DTXCID8029367 \| 2,3-Benzodiazine \| NSC62484 \| NSC-62484 \| InChI=1/C8H6N2/c1-2-4-8-6-10-9-5-7(8)3-1/h1-6 \| P0694 \| AKOS009157299 \| phthalazin \| AS-15090 \| CS-W002016 \| EINECS 205-963-2 \| Phthalazine, 98%
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Application： Phthalazine derivatives including copper and platinum complexes were induce the apoptosis in breast cancer cell lines and renal hyperemia.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Diazanaphthalenes
    - Subclass Benzodiazines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Diazanaphthalenes
Subclass	Benzodiazines
Intermediate Tree Nodes	Not available
Direct Parent	Phthalazines
Alternative Parents	Pyridazines and derivatives Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Phthalazine - Benzenoid - Pyridazine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as phthalazines. These are compounds containing a phthalazine moiety, which consists of a benzene ring fused to a pyridazine, forming a 2,3-benzodiazine skeleton.
External Descriptors	mancude organic heterobicyclic parent - phthalazines - azaarene - ortho-fused heteroarene
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

AOX1 Tchem Aldehyde oxidase (429 Activities)

Discover Target: AOX1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

PTR1 Pteridine reductase 1 (345 Activities)

Discover Target: PTR1

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

Pubchem Sid	488180941
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488180941
IUPAC Name	phthalazine
INCHI	InChI=1S/C8H6N2/c1-2-4-8-6-10-9-5-7(8)3-1/h1-6H
InChIKey	LFSXCDWNBUNEEM-UHFFFAOYSA-N
Smiles	C1=CC=C2C=NN=CC2=C1
Isomeric SMILES	C1=CC=C2C=NN=CC2=C1
WGK Germany	3
PubChem CID	9207
Molecular Weight	130.15
Beilstein	23174
Reaxy-Rn	109240

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.

22 results found

Lot Number	Certificate Type	Date	Item
K2307155	Certificate of Analysis	Oct 14, 2023	P160145
K2307159	Certificate of Analysis	Oct 14, 2023	P160145
E2310824	Certificate of Analysis	Nov 16, 2022	P160145
E2310835	Certificate of Analysis	Nov 16, 2022	P160145
E2310831	Certificate of Analysis	Nov 16, 2022	P160145
E2310837	Certificate of Analysis	Nov 16, 2022	P160145
E2310896	Certificate of Analysis	Nov 16, 2022	P160145
E2310829	Certificate of Analysis	Nov 16, 2022	P160145
E2310832	Certificate of Analysis	Nov 16, 2022	P160145
E2310828	Certificate of Analysis	Nov 16, 2022	P160145
K1830039	Certificate of Analysis	Sep 20, 2022	P160145
K1830038	Certificate of Analysis	Sep 20, 2022	P160145
F2222471	Certificate of Analysis	Jun 29, 2022	P160145
F2205302	Certificate of Analysis	Jun 07, 2022	P160145
C2224046	Certificate of Analysis	May 30, 2022	P160145
F2222448	Certificate of Analysis	May 20, 2022	P160145
C2224048	Certificate of Analysis	May 20, 2022	P160145
F2205304	Certificate of Analysis	May 20, 2022	P160145
E2225045	Certificate of Analysis	Mar 04, 2022	P160145
E2225036	Certificate of Analysis	Mar 04, 2022	P160145
E2225037	Certificate of Analysis	Mar 04, 2022	P160145
E2225033	Certificate of Analysis	Mar 04, 2022	P160145

Show more⌵

Chemical and Physical Properties

Solubility	Soluble in water; Soluble in Alcohol,Benzene
Boil Point(°C)	189 °C
Melt Point(°C)	89-92°C
Molecular Weight	130.150 g/mol
XLogP3	0.600
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	130.053 Da
Monoisotopic Mass	130.053 Da
Topological Polar Surface Area	25.800 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	99.800
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Yifan Li, Chang Chen, Rui Cao, Ziwei Pan, Hua He, Kebin Zhou. (2020) Dual-atom Ag2/graphene catalyst for efficient electroreduction of CO2 to CO. APPLIED CATALYSIS B-ENVIRONMENTAL, 268 (118747).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.