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Merck

15404

Sigma-Aldrich

N-Boc-1,4-butandiamin

≥97.0% (GC/NT)

Synonym(e):

N-(4-Aminobutyl)-carbamidsäure-tert.-butylester, N-Boc-1,4-diamino-butan

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About This Item

Lineare Formel:
(CH3)3COCONH(CH2)4NH2
CAS-Nummer:
Molekulargewicht:
188.27
Beilstein:
1937878
MDL-Nummer:
UNSPSC-Code:
12352116
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

Assay

≥97.0% (GC/NT)

Eignung der Reaktion

reagent type: cross-linking reagent

Brechungsindex

n20/D 1.460

Dichte

0.984 g/mL at 20 °C (lit.)

Funktionelle Gruppe

Boc
amine

SMILES String

NCCCCNC(OC(C)(C)C)=O

InChI

1S/C9H20N2O2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7,10H2,1-3H3,(H,11,12)

InChIKey

ZFQWJXFJJZUVPI-UHFFFAOYSA-N

Verwandte Kategorien

Anwendung

  • Carboxy-Silane Coated Iron Oxide Nanoparticles: Details the application of N-Boc-1,4-butanediamine in modifying iron oxide nanoparticles for imaging and drug delivery (D Stanicki, S Boutry, S Laurent, et al., 2014). Access the article.

Sonstige Hinweise

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

Piktogramme

Corrosion

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

228.2 °F - closed cup

Flammpunkt (°C)

109.0 °C - closed cup

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Mono-Boc-protected diamines are versatile building blocks for chemical synthesis. Their production is a lot more challenging than the simple reaction scheme might imply, because the Boc-anhydride reagent cannot differentiate between the two identical amino moieties in the substrate.

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