Identification | Back Directory | [Name]
BIS- BOC-SPERMIDINE | [CAS]
68076-39-1 | [Synonyms]
BIS- BOC-SPERMIDINE N1,N5-bis-Boc-sperMidine 1,6-bis-Boc-1,6,10-triazadecane N1,N5-Bis-Boc-spermidine >=95.0% (TLC) N-(3-AMINOPROPYL)-N,N’-DIBOC-DIAMINOBUTANE N1,N5-Bis-Boc-sperMidine Tert-Butyl (3-aminopropyl)(4-((tert-butoxycarbonyl)amino)butyl)carbamate tert-butyl N-(3-aminopropyl)-N-(4-{[(tert-butoxy)carbonyl]amino}butyl)carbamate tert-butylN-[4-(3-aminopropylamino)butyl]-N-[(2-methylpropan-2-yl)oxycarbonyl]carbamate Carbamic acid, (3-aminopropyl)[4-[[(1,1-dimethylethoxy)carbonyl]amino]butyl]-, 1,1-dimethylethyl ester Carbamic acid, N-(3-aminopropyl)-N-[4-[[(1,1-dimethylethoxy)carbonyl]amino]butyl]-, 1,1-dimethylethyl ester | [Molecular Formula]
C17H35N3O4 | [MDL Number]
MFCD04973457 | [MOL File]
68076-39-1.mol | [Molecular Weight]
345.48 |
Chemical Properties | Back Directory | [Boiling point ]
462.0±38.0 °C(Predicted) | [density ]
1.028±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C | [pka]
12.87±0.46(Predicted) | [BRN ]
2059741 |
Hazard Information | Back Directory | [Description]
N1,N5-Bis-Boc-spermidine is a linker containing an amino group with two Boc-protected amino groups. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine. | [Chemical Properties]
Light yellow viscid liquid |
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