N-Boc-1,3-propanediamine
ALDRICH/15408 - ≥97.0% (GC/NT)
Synonym: N-
CAS Number: 75178-96-0
Empirical Formula (Hill Notation): C8H18N2O2
Molecular Weight: 174.24
MDL Number: MFCD00210021
Linear Formula: (CH3)3COCONH(CH2)3NH2
Product Type: Chemical
| assay | ≥97.0% (GC/NT) |
| bp | 203 °C (lit.) |
| density | 0.998 g/mL at 20 °C (lit.) |
| functional group | amine |
| Boc | |
| InChI | 1S/C8H18N2O2/c1-8(2,3)12- |
| InChI key | POHWAQLZBIMPRN-UHFFFAOYSA |
| mp | 22 °C (lit.) |
| Quality Level | 100 ![]() |
| reaction suitability | reagent type: cross-linking reagent |
| refractive index | n |
| n |
|
| SMILES string | NCCCNC(OC(C)(C)C)=O |
| Application: | • Tackling vancomycin-resistant bacteria with ′lipophilic–vancomycin–ca![]() • Sulfonamides differing in the alkylamino substituent length–Synthesis, electrochemical characteristic, acid-base profile and complexation properties: The study involves N-Boc-1,3-propanediamine in the synthesis of novel sulfonamide derivatives with potential biochemical applications (Ciesielska et al., 2022 ![]() • Direct α-alkylation of primary aliphatic amines enabled by CO2 and electrostatics: Research demonstrating selective α-alkylation of N-Boc-1,3-propanediamine, highlighting a novel method in organic synthesis (Ye et al., 2018 ![]() |
| Other Notes: | Synthesis of spermidine analogues; Preparation of pharmacologically active compounds. |
| Packaging: | 1, 5 mL in glass bottle |
| Symbol | ![]() GHS05,GHS07 |
| Signal word | Danger |
| Hazard statements | H302 - H314 |
| Precautionary statements | P280 - P305 + P351 + P338 - P310 |
| Hazard Codes | C |
| Risk Statements | 22-34 |
| Safety Statements | 26-36/37/39-45 |
| RIDADR | UN 3259PSN1 8 / PGIII |
| WGK Germany | WGK 3 |
| Flash Point(F) | 228.2 °F - closed cup |
| Flash Point(C) | 109 °C - closed cup |
| Purity | ≥97.0% (GC/NT) |
| bp | 203 °C (lit.) |
| mp | 22 °C (lit.) |
| Density | 0.998 g/mL at 20 °C (lit.) |
| Refractive Index | n |
| UNSPSC | 12352116 |



