Ordering
Available Variants1 g
CHA.24841-1g
Price
€92.00
Available – Dispatch in 14 days
5 g
CHA.24841-5g
Price
€199.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.24841-1g | €92.00 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.24841-5g | €199.20 |
96%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | IC6H4CH2NH2 |
|---|---|
| CAS Number | 696-40-2 |
| Molecular Weight | 233.05 |
| NACRES | NA.22 |
| PubChem Substance ID | 24846513 |
| UNSPSC Code | 12352100 |
| MDL number | MFCD00192227 |
| Assay | 96% |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS08
GHS07
  GHS08,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H315,H317,H319,H334,H335,H361 |
| pcodes | P202 - P261 - P280 - P302 + P352 - P305 + P351 + P338 - P308 + P313 |
| Hazard Classifications | Eye Irrit. 2 - Repr. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3 |
| target_organs | Respiratory system |
| wgk | WGK 3 |
| flash_point_f | >235.4 °F - closed cup |
| flash_point_c | > 113 °C - closed cup |
| ppe | dust mask type N95 (US), Eyeshields, Faceshields, Gloves |
| Storage Class | 10 - Combustible liquids |
Technical Overview & Applications Use-case context
3-Iodobenzylamine, with the CAS registry number 696-40-2, is an organic compound that has been utilized in various chemical synthesis applications. This aromatic amine derivative is characterized by the presence of an iodine atom attached to a benzyl group, which is further functionalized with an amine moiety. The compounds unique structure renders it a valuable intermediate in the preparation of more complex molecules, including pharmaceuticals and materials science-related compounds. Its reactivity profile, which includes susceptibility to nucleophilic substitution and cross-coupling reactions, makes it a versatile building block for the construction of diverse chemical architectures. As such, 3-iodobenzylamine has garnered significant attention in the scientific community, with its potential applications spanning multiple disciplines, from medicinal chemistry to advanced materials design.
