4-Aminobenzylamine
4-Aminobenzylamine structure
|
Common Name | 4-Aminobenzylamine | ||
|---|---|---|---|---|
| CAS Number | 4403-71-8 | Molecular Weight | 122.16800 | |
| Density | 1.078 g/mL at 25 °C(lit.) | Boiling Point | 101 °C0.05 mm Hg(lit.) | |
| Molecular Formula | C7H10N2 | Melting Point | 37 °C | |
| MSDS | Chinese USA | Flash Point | >230 °F | |
| Symbol |
GHS05 |
Signal Word | Danger | |
| Name | 4-Aminobenzylamine |
|---|---|
| Synonym | More Synonyms |
| Density | 1.078 g/mL at 25 °C(lit.) |
|---|---|
| Boiling Point | 101 °C0.05 mm Hg(lit.) |
| Melting Point | 37 °C |
| Molecular Formula | C7H10N2 |
| Molecular Weight | 122.16800 |
| Flash Point | >230 °F |
| Exact Mass | 122.08400 |
| PSA | 52.04000 |
| LogP | 2.00900 |
| Index of Refraction | n20/D 1.61(lit.) |
| InChIKey | BFWYZZPDZZGSLJ-UHFFFAOYSA-N |
| SMILES | NCc1ccc(N)cc1 |
| Symbol |
GHS05 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H314 |
| Precautionary Statements | P280-P305 + P351 + P338-P310 |
| Personal Protective Equipment | Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
| Hazard Codes | C:Corrosive; |
| Risk Phrases | R34 |
| Safety Phrases | S26-S28-S36/37/39-S45 |
| RIDADR | UN 3259 8/PG 2 |
| WGK Germany | 3 |
| Packaging Group | III |
| Hazard Class | 8 |
| HS Code | 2921590090 |
| Precursor 10 | |
|---|---|
| DownStream 10 | |
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CAS#:32478-65-2| HS Code | 2921590090 |
|---|---|
| Summary | 2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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Highly sensitive electrochemical biosensor for bisphenol A detection based on a diazonium-functionalized boron-doped diamond electrode modified with a multi-walled carbon nanotube-tyrosinase hybrid film.
Biosens. Bioelectron. 74 , 830-5, (2015) A highly sensitive electrochemical biosensor for the detection of Bisphenol A (BPA) in water has been developed by immobilizing tyrosinase onto a diazonium-functionalized boron doped diamond electrode... |
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Modification of carbon electrode with aryl groups having an aliphatic amine by electrochemical reduction of in situ generated diazonium cations.
Langmuir 24(16) , 8711-8, (2008) The electrochemically induced functionalization of glassy carbon electrode by aryl groups having an aliphatic amine group was achieved by reduction of in situ generated diazonium cations in aqueous me... |
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Electrochemical modification of single carbon nanotubes.
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