| Identification | Back Directory | [Name]
1-Propanamine, 3-azido- | [CAS]
88192-19-2 | [Synonyms]
3-azido-
Azido-Propylamine
3-AzidopropylaMine
3-Aminopropyl Azide
3-Azido-1-propylamine
3-Azido-1-propanamine
3-Azidopropyl-1-aMine
3-AZIDOPROPAN-1-AMINE
3-Azidopropylamine >
3-Azidopropyl-1-amine3
1-Amino-3-azidopropane
1-Propanamine, 3-azido-
3-Azido-propylamine HCl
3-Azido-1-propanamine 90%
3-azidopropan-1-amine HCl
3-Azidopropyl-1-amine - A2033 | [Molecular Formula]
C3H8N4 | [MDL Number]
MFCD11046568 | [MOL File]
88192-19-2.mol | [Molecular Weight]
100.12 |
| Chemical Properties | Back Directory | [Melting point ]
47-49 °C | [Boiling point ]
50°C/15mmHg(lit.) | [density ]
1.020 g/mL at 25 °C | [refractive index ]
n20/D1.471 | [Fp ]
60°(140°F) | [storage temp. ]
?20°C | [form ]
Liquid | [color ]
Pale Yellow | [Water Solubility ]
Soluble in DMSO, DMF, DCM, chloroform, THF, and water.Miscible with dimethylsulfoxide, dimethyl formamide, dichloromethane, tetrahydrofuran, chloroform and water. | [InChI]
InChI=1S/C3H8N4/c4-2-1-3-6-7-5/h1-4H2 | [InChIKey]
OYBOVXXFJYJYPC-UHFFFAOYSA-N | [SMILES]
NCCCN=[N+]=[N-] |
| Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
25 | [Safety Statements ]
45 | [RIDADR ]
UN 1992 6.1(3) / PGIII | [WGK Germany ]
3 | [HS Code ]
2929.90.5090 | [HazardClass ]
3 | [PackingGroup ]
III |
| Hazard Information | Back Directory | [Uses]
Amine modified azide for click chemistry. | [Uses]
Azido-containing reagent with carbonyl and carboxyl reactivity3-Azido-1-propylamine is used in the preparation of perylenedimides derivative by reacting with 1,6,7,12-tetrachloroperylene-3,4:9,10-tetracarboxyanhydride, which is used in click chemistry. | [General Description]
3-Azido-1-propanamine can be used to functionalize:
- Bismethylolpropionic acid (bis-MPA) monomers with azide functional group to generate high-generation dendrimers.,
- Clickable zinc tetraphenylporphyrin scaffold with an azido group through click chemistry applicable in photodynamic therapy.
| [reaction suitability]
reaction type: click chemistry |
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