≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Application:
3,4,5,6-Tetrachlorophthalimide was used to study the influence of metal binding and posttranslational modification of the carboxylated lysine on the activity of recombinant hydantoinase from Agrobacterium radiobacter.
| Pubchem Sid | 488184862 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184862 |
| Canonical Smiles | C12=C(C(=C(C(=C1Cl)Cl)Cl)Cl)C(=O)NC2=O |
| IUPAC Name | 4,5,6,7-tetrachloroisoindole-1,3-dione |
| InChIKey | LPUUYZVKCMCHLO-UHFFFAOYSA-N |
| INCHI | 1S/C8HCl4NO2/c9-3-1-2(8(15)13-7(1)14)4(10)6(12)5(3)11/h(H,13,14,15) |
| Isomeric SMILES | C12=C(C(=C(C(=C1Cl)Cl)Cl)Cl)C(=O)NC2=O |
| WGK Germany | 3 |
| PubChem CID | 74077 |
| Molecular Weight | 284.9 |
| Beilstein | 21505 |
| Reaxy-Rn | 211580 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Isoindoles and derivatives |
| Subclass | Isoindolines |
| Intermediate Tree Nodes | Isoindolones |
| Direct Parent | Phthalimides |
| Alternative Parents | Isoindoles Benzenoids Aryl chlorides Vinylogous halides N-unsubstituted carboxylic acid imides Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Phthalimide - Isoindole - Aryl chloride - Aryl halide - Benzenoid - Carboxylic acid imide - Vinylogous halide - Carboxylic acid imide, n-unsubstituted - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - 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 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 K2203306 | Certificate of Analysis | Jul 30, 2026 | T161532 |
| K2203307 | Certificate of Analysis | Jul 30, 2026 | T161532 |
| K2203308 | Certificate of Analysis | Jul 30, 2026 | T161532 |
| K2203309 | Certificate of Analysis | Jul 30, 2026 | T161532 |
| G2411477 | Certificate of Analysis | Jun 12, 2024 | T161532 |
| G2411483 | Certificate of Analysis | Jun 12, 2024 | T161532 |
| Solubility | DMF: soluble 25 mg/mL, clear, light yellow |
|---|---|
| Melt Point(°C) | 339°C(lit.) |
| Molecular Weight | 284.900 g/mol |
| XLogP3 | 3.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 284.873 Da |
| Monoisotopic Mass | 282.876 Da |
| Topological Polar Surface Area | 46.200 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 294.000 |
| 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 |
