| N-Boc-1,3-propanediamine Basic information |
| Product Name: | N-Boc-1,3-propanediamine |
| Synonyms: | Boc-DAP;N-t-Butyloxycarbonyl-1,3-diaminopropane;N-(3-Aminopropyl)carbamic acid tert-butyl ester ,98%;N-(3-Aminopropyl)carbamic Acid tert-Butyl Ester N-Boc-1,3-diaminopropane N-Boc-1,3-propanediamine N-(tert-Butoxycarbonyl)-1,3-propanediamine tert-Butyl N-(3-Aminopropyl)carbamate;tert-Butyl N-(3-aMiNApropyl)carbaMate;N-Boc-1,3-propanediaMine (N-Boc-1,3-diaMinopropane;N-(3-Aminopropyl)carbamic acid tert-butyl ester ,85%;tert-butyl (3-aminopropyl)carbamate(SALTDATA: FREE) |
| CAS: | 75178-96-0 |
| MF: | C8H18N2O2 |
| MW: | 174.24 |
| EINECS: | 628-600-3 |
| Product Categories: | Amines and Anilines;N-BOC;Monoprotected Diaminoalkanes;N-Boc-diaminoalkanes;Bifunctional Linkers;Building Blocks;pharmacetical;Chemical Biology;Chemical Synthesis;Linkers and Crosslinkers;Nitrogen Compounds;Organic Building Blocks;Protected Amines |
| Mol File: | 75178-96-0.mol |
| N-Boc-1,3-propanediamine Chemical Properties |
| Melting point | 22 °C (lit.) |
| Boiling point | 203 °C (lit.) |
| density | 0.998 g/mL at 20 °C (lit.) |
| refractive index | n |
| Fp | >230 °F |
| storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C |
| solubility | Miscible with methanol. |
| pka | 12.73±0.46(Predicted) |
| form | Liquid |
| Specific Gravity | 0.998 |
| color | Colorless |
| Sensitive | Air Sensitive |
| BRN | 3588328 |
| InChIKey | POHWAQLZBIMPRN-UHFFFAOYSA-N |
| CAS DataBase Reference | 75178-96-0(CAS DataBase Reference) |
| Safety Information |
| Hazard Codes | C |
| Risk Statements | 22-34 |
| Safety Statements | 26-36/37/39-45 |
| RIDADR | UN 3259 8/PG 3 |
| WGK Germany | 3 |
| F | 10-34 |
| Hazard Note | Irritant |
| HazardClass | 8 |
| PackingGroup | III |
| HS Code | 29212900 |
| MSDS Information |
| Provider | Language |
|---|---|
| SigmaAldrich | English |
| ALFA | English |
| N-Boc-1,3-propanediamine Usage And Synthesis |
| Chemical Properties | Colorless to light yellow liquid |
| Uses | N-Boc-1,3-diaminopropane is used in the preparation of spermidine analogues as well as in the preparation of pharmacologically active compounds. It is also used in suzuki reaction. Further, it is used in the preparation of [3-(3-cyano-propylamino)-propyl]-carbamic acid tert-butyl ester. |
| Uses | suzuki reaction |
| N-Boc-1,3-propanediamine Preparation Products And Raw materials |
| Raw materials | Ethanol-->Sodium hydroxide-->Hydrochloric acid-->Methanol-->Dichloromethane-->Acetic acid-->Chloroform-->Di-tert-butyl dicarbonate-->Ethylenediamine-->1,3-Diaminopropane |
| Preparation Products | BIS- BOC-SPERMIDINE |
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