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≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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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.
4-Iodobenzylamine hydrochloride can be synthesized in three steps from 4-iodobenzoic acid
| Pubchem Sid | 488199233 |
|---|---|
| Sonrisas canónicas | C1=CC(=CC=C1CN)I.Cl |
| IUPAC Name | (4-iodophenyl)methanamine;hydrochloride |
| InChIKey | GBJMURRFWZREHE-UHFFFAOYSA-N |
| INCHI | 1S/C7H8IN.ClH/c8-7-3-1-6(5-9)2-4-7;/h1-4H,5,9H2;1H |
| Isómeros SMILES | C1=CC(=CC=C1CN)I.Cl |
| WGK Alemania | 3 |
| PubChem CID | 16217505 |
| Peso molecular | 269.51 |
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 | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Phenylmethylamines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylmethylamines |
| Alternative Parents | Benzylamines Iodobenzenes Aralkylamines Aryl iodides Organopnictogen compounds Organoiodides Organic chloride salts Monoalkylamines Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Benzylamine - Phenylmethylamine - Halobenzene - Aralkylamine - Iodobenzene - Aryl halide - Aryl iodide - Amine - Primary amine - Organonitrogen compound - Organoiodide - Organohalogen compound - Primary aliphatic amine - Organic salt - Organic chloride salt - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as phenylmethylamines. These are compounds containing a phenylmethtylamine moiety, which consists of a phenyl group substituted by an methanamine. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Apr 03, 2026 | I171122 | |
| Certificate of Analysis | Apr 03, 2026 | I171122 | |
| Certificate of Analysis | Apr 03, 2026 | I171122 | |
| Certificate of Analysis | Mar 24, 2025 | I171122 | |
| Certificate of Analysis | Jan 03, 2025 | I171122 |
| Solubilidad | Soluble in water. |
|---|---|
| Sensibilidad | Light sensitive;Hygroscopic |
| Punto de fusión (°C) | 299-303°C |
| Peso molecular | 269.510 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 268.947 Da |
| Monoisotopic Mass | 268.947 Da |
| Topological Polar Surface Area | 26.000 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 77.000 |
| 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 | 2 |