- 4-Aminobenzylamine
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- $0.00 / 25kg
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2025-12-01
- CAS:4403-71-8
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 10000KGS
- 4-Aminobenzylamine
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- $1.00 / 1KG
-
2019-12-26
- CAS:4403-71-8
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: Customized
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| | 4-Aminobenzylamine Basic information |
| | 4-Aminobenzylamine Chemical Properties |
| Melting point | 37 °C | | Boiling point | 101 °C/0.05 mmHg (lit.) | | density | 1.078 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.61(lit.) | | Fp | >230 °F | | storage temp. | 2-8°C, protect from light | | pka | 9.65±0.10(Predicted) | | form | Oily Liquid | | color | Clear light brown to brown | | λmax | 246nm(EtOH)(lit.) | | InChI | 1S/C7H10N2/c8-5-6-1-3-7(9)4-2-6/h1-4H,5,8-9H2 | | InChIKey | BFWYZZPDZZGSLJ-UHFFFAOYSA-N | | SMILES | NCc1ccc(N)cc1 | | CAS DataBase Reference | 4403-71-8(CAS DataBase Reference) |
| Hazard Codes | C | | Risk Statements | 34 | | Safety Statements | 26-28-36/37/39-45 | | RIDADR | UN 3259 8/PG 2 | | WGK Germany | 3 | | Hazard Note | Corrosive | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29215990 | | Storage Class | 8A - Combustible corrosive hazardous materials | | Hazard Classifications | Skin Corr. 1B |
| | 4-Aminobenzylamine Usage And Synthesis |
| Chemical Properties | white to light yellow crystal powde | | Uses | 4-Aminobenzylamine may be used:
- in the electrochemical modification of single-walled carbon nanotubes (SWCNTs), via oxidative coupling
- in the preparation of a novel acridine-based amino acid
- in the synthesis of two novel fluorescent Photoinduced Electron Transfer (PET) anion sensors, based on the principle of ′fluorophore-spacer-(anion)receptor′
- in anodic coupling of SWCNTs
- in the synthesis of polyacrylamide series containing salicylideneaniline moieties, by a double polymer analogous reaction with reactive precursor polymer poly(pentafluorophenylacrylate) (PPFPA)
| | General Description | 4-Aminobenzylamine is an aromatic amine. Diazonium cations of 4-aminobenzylamine were generated in situ with sodium nitrite in aqueous HCl, which were used for the modification of glassy carbon electrode by aryl groups having an aliphatic amine group. |
| | 4-Aminobenzylamine Preparation Products And Raw materials |
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