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15404 Sigma-Aldrich

N-Boc-1,4-butanediamine

≥97.0% (GC/NT)

Synonym: N-Boc-1,4-diaminobutane, tert-Butyl N-(4-aminobutyl)carbamate

  • CAS Number 68076-36-8

  • Linear Formula (CH3)3COCONH(CH2)4NH2

  • Molecular Weight 188.27

  •  Beilstein/REAXYS Number 1937878

  •  MDL number MFCD00210019

  •  PubChem Substance ID 57647412

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Properties

Related Categories Bifunctional Linkers, Building Blocks, Chemical Biology, Chemical Synthesis, Linkers and Crosslinkers,
Quality Level   100
assay   ≥97.0% (GC/NT)
reaction suitability   reagent type: cross-linking reagent
refractive index   n20/D 1.460
density   0.984 g/mL at 20 °C (lit.)
SMILES string   CC(C)(C)OC(=O)NCCCCN
InChI   1S/C9H20N2O2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7,10H2,1-3H3,(H,11,12)
InChI key   ZFQWJXFJJZUVPI-UHFFFAOYSA-N

Description

Packaging

1, 5 mL in glass bottle

Other Notes

Preparation of pharmacologically active compounds. Preparation of spermidine analogues. Introduction of a C4-spacer.

Safety & Documentation

Safety Information

Symbol 
GHS05  GHS05
Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
UN 2735PSN2 8 / PGIII
WGK Germany 
WGK 3
Flash Point(F) 
228.2 °F - closed cup
Flash Point(C) 
109.0 °C - closed cup

Documents

Certificate of Analysis (COA)

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Protocols & Articles

Articles

MRT - Mono-Boc-Protection of Diamines

Benefit from MRT & Flow Chemistry: Green production of a highly pure product with 100% yield thanks to precise control over reaction temperature.
Matthias Junkers
Aldrich ChemFiles 2009, 9.4, 12.
Keywords: Building blocks, Continuous flow chemistry, Microreactor technology, Precipitation, Solvents

Mono-Protected Diaminoalkanes

Mono-Boc-protected diaminoalkanes are very useful for the introduction of homobifunctional spacers in many different applications. Additionally, they play an important role as building blocks in the ...
ChemFiles Volume 3 Article 4
Keywords: Applications, Building blocks

Peer-Reviewed Papers
15

References

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