Skip to the beginning of the images gallery

4-Nitrophthalimide - >98.0%(HPLC), high purity , CAS No.89-40-7

6 Citations

COA

Grade & Purity:

≥98%(HPLC)

Cas Number: 89-40-7
Molecular Weight: 192.13
Beilstein Registry Number: 21(2)373
MDL number: MFCD00005884
PubChem CID: 6969
PubChem SID: 488180224

In stock

Item Number

N158906

Grouped product items
SKU	Size	Availability	Price
N158906-5g	5g	2	$9.90
N158906-25g	25g	2	$23.90
N158906-100g	100g	3	$85.90
N158906-250g	250g	5	$192.90
N158906-500g	500g	1	$234.90

View related series

Nitrogenous compounds (2445) Non heterocyclic block (8163)

Basic Description

Synonyms	F0345-4666 \| 1H-Isoindole-1,3(2H)-dione, 5-nitro- \| CAS-89-40-7 \| AKOS000313129 \| 4-Nitrophthalimide, 98% \| W-100375 \| NSC 5394 \| EN300-16888 \| 5-Nitrophthalimide \| 5-nitro-phthalimide \| SCHEMBL16303093 \| D70991 \| 4-NITROPHTHALIMIDE \| 4-nitro-phthalimide
Specifications & Purity	≥98%(HPLC)
Shipped In	Normal
Product Description	Application： diagnostic assay manufacturing hematology histology

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Isoindoles and derivatives
    - Subclass Isoindolines
      - Level5 Isoindolones
        Level6 Phthalimides

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Isoindoles and derivatives
Subclass	Isoindolines
Intermediate Tree Nodes	Isoindolones
Direct Parent	Phthalimides
Alternative Parents	Isoindoles Nitroaromatic compounds Benzenoids N-unsubstituted carboxylic acid imides Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Phthalimide - Isoindole - Nitroaromatic compound - Benzenoid - Carboxylic acid imide - Carboxylic acid imide, n-unsubstituted - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides.
External Descriptors	Not available
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)

XDH Tclin Xanthine dehydrogenase (1038 Activities)

Discover Target: XDH

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

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

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	488180224
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488180224
IUPAC Name	5-nitroisoindole-1,3-dione
INCHI	InChI=1S/C8H4N2O4/c11-7-5-2-1-4(10(13)14)3-6(5)8(12)9-7/h1-3H,(H,9,11,12)
InChIKey	ANYWGXDASKQYAD-UHFFFAOYSA-N
Smiles	C1=CC2=C(C=C1[N+](=O)[O-])C(=O)NC2=O
Isomeric SMILES	C1=CC2=C(C=C1[N+](=O)[O-])C(=O)NC2=O
RTECS	TI5625000
Molecular Weight	192.13
Beilstein	21(2)373
Reaxy-Rn	180224
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=180224&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.

10 results found

Lot Number	Certificate Type	Date	Item
C1919051	Certificate of Analysis	Jan 10, 2023	N158906
L2201460	Certificate of Analysis	Nov 02, 2022	N158906
L2201458	Certificate of Analysis	Nov 02, 2022	N158906
L2201459	Certificate of Analysis	Nov 02, 2022	N158906
L2201457	Certificate of Analysis	Nov 02, 2022	N158906
L2201463	Certificate of Analysis	Nov 02, 2022	N158906
L2201464	Certificate of Analysis	Nov 02, 2022	N158906
L2201461	Certificate of Analysis	Nov 02, 2022	N158906
L2201462	Certificate of Analysis	Nov 02, 2022	N158906
J2211505	Certificate of Analysis	Jun 19, 2021	N158906

Chemical and Physical Properties

Melt Point(°C)	202 °C
Molecular Weight	192.130 g/mol
XLogP3	1.000
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	0
Exact Mass	192.017 Da
Monoisotopic Mass	192.017 Da
Topological Polar Surface Area	92.000 Å²
Heavy Atom Count	14
Formal Charge	0
Complexity	309.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Yuxia Liu, Wensi Xu, Wenfeng Zhuge, Qing Huang, Gang Xiang, Jinyun Peng. (2023) Conductive aluminum phthalocyanine-based porous organic polymer as an efficient electrocatalyst for nifedipine detection. SENSORS AND ACTUATORS B-CHEMICAL, (135191).
2. Gang Xiang, Wensi Xu, Wenfeng Zhuge, Qing Huang, Cuizhong Zhang, Jinyun Peng. (2023) Conductive phthalocyanine-based porous organic polymer as sensing platform for rapid determination of vanillin. ANALYST, 148 (24): (6274-6281).
3. Yan Gao, Liangting Chen, Guangfa Hu, Xiao Wang, Gai Zhang, Ying Zheng, Jianshe Zhao. (2019) Amino-substituted binuclear phthalocyanines bonding with multi-wall carbon nanotube as efficient electrocatalysts for lithium-thionyl chloride battery. JOURNAL OF MATERIALS RESEARCH, 34 (6): (921-931).
4. Na Zhao, Siwen Li, Jinyi Wang, Ronglan Zhang, Ruimin Gao, Jianshe Zhao, Junlong Wang. (2015) Synthesis and application of different phthalocyanine molecular sieve catalyst for oxidative desulfurization. JOURNAL OF SOLID STATE CHEMISTRY, 225 (347).
5. Xiaofei Zhang, Haitao Liu, Pengfei An, Yanan Shi, Jianyu Han, Zhongjie Yang, Chang Long, Jun Guo, Shenlong Zhao, Kun Zhao, Huajie Yin, Lirong Zheng, Binhao Zhang, Xiaoping Liu, Lijuan Zhang, Guodong Li, Zhiyong Tang,. (2020-05-20) Delocalized electron effect on single metal sites in ultrathin conjugated microporous polymer nanosheets for boosting CO2 cycloaddition.. Science advances, 6 ((17)): ( eaaz4824-eaaz4824 ).
6. Gang Xiang, Wensi Xu, Wenfeng Zhuge, Qing Huang, Cuizhong Zhang, Jinyun Peng. (2024) A Tröger's base-linked aluminium phthalocyanine polymer for discriminative electrochemical sensing of the antibiotic isoniazid. Analytical Methods, 16 (7): (1012-1020).

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