| Identification | Back Directory | [Name]
BOC-BIOCYTIN | [CAS]
62062-43-5 | [Synonyms]
BOC-BCT-OH
BOC-BIOCYTIN
nα-boc-biocytin
N-T-BOC-BIOCYTIN
BOC-LYS(BIOT)-OH
BOC-LYS(BIOTIN)-OH
BOC-L-LYS(BIOTIN)-OH
BOC-LYS(BIOTINYL)-OH
N-ALPHA-BOC-BIOCYTIN
Boc-L-Lys(biotinyl)-OH
BOC-LYSINE(BIOTINYL)-OH
nα-boc-nε-biotinyl-l-lysine
BOC-LYS(EPSILON-D-BIOTIN)-OH
BOC-N-EPSILON-BIOTINYL-L-LYSINE
Nα-Boc-Nε-biotinyl-L-lysine98+%
N-(tert-butoxycarbonyl)biocytin
Nα-Boc-biocytin [t-Boc-Biocytin]
N-ALPHA-T-BUTOXYCARBONYL-L-BIOCYTIN
N-EPSILON-BIOTINYL-N-ALPHA-BOC-L-LYSINE
N-ALPHA-T-BOC-N-EPSILON-(D-BIOTIN)-L-LYSINE
N-ALPHA-T-BUTOXYCARBONYL-N-EPSILON-BIOTINYL-L-LYSINE
N-ALPHA-T-BUTYLOXYCARBONYL-N-EPSILON-BIOTINYL-L-LYSINE
N-ALPHA-TERT-BUTYLOXYCARBONYL-N-EPSILON-BIOTINYL-L-LYSINE
Nα-Boc-Nε-biotinyl-L-lysine, Nε-Biotinyl-Nα-Boc-L-lysine
N2-[(1,1-DiMethylethoxy)carbonyl]-N6-[5-[(3aS,4S,6aR)-hexahydro-2-oxo-1H-thieno[3,4-d]iMidazol-4-yl]-1-oxopentyl]-L-lysine
REF DUPL: (S)-1-(9H-fluoren-9-yl)-3,11,18-trioxo-22-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)-2-oxa-4,10,17-triazadocosane-5-carboxylic acid | [Molecular Formula]
C21H36N4O6S | [MDL Number]
MFCD00133628 | [MOL File]
62062-43-5.mol | [Molecular Weight]
472.6 |
| Chemical Properties | Back Directory | [Appearance]
White Solid | [Melting point ]
132 | [Boiling point ]
799.5°C at 760 mmHg | [density ]
1.202 g/cm3 | [storage temp. ]
-15°C | [solubility ]
DMSO, Methanol | [form ]
Solid | [color ]
White | [BRN ]
5797526 | [Major Application]
peptide synthesis | [InChIKey]
XTQNFOCBPUXJCS-JKQORVJESA-N | [SMILES]
[H][C@]12CS[C@@H](CCCCC(=O)NCCCC[C@H](NC(=O)OC(C)(C)C)C(O)=O)[C@@]1([H])NC(=O)N2 |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
An intermediate in the synthesis of biocytin-containing peptides | [Description]
N-Boc-Biocytin is a biotin PEG linker containing a carboxylic group and Boc-protected amine. Reaction of carboxylic with primary amino (-NH2) forms stable, irreversible amide bonds. The Boc group can be deprotected under acidic condition to obtain the free amine which can be used for further conjugations. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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