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15404

Sigma-Aldrich

N-Boc-1,4-butanediamine

≥97.0% (GC/NT)

Synonyme(s) :

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

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About This Item

Formule linéaire :
(CH3)3COCONH(CH2)4NH2
Numéro CAS:
Poids moléculaire :
188.27
Numéro Beilstein :
1937878
Numéro MDL:
Code UNSPSC :
12352116
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Niveau de qualité

Pureté

≥97.0% (GC/NT)

Pertinence de la réaction

reagent type: cross-linking reagent

Indice de réfraction

n20/D 1.460

Densité

0.984 g/mL at 20 °C (lit.)

Groupe fonctionnel

Boc
amine

Chaîne SMILES 

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)

Clé InChI

ZFQWJXFJJZUVPI-UHFFFAOYSA-N

Application

  • 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.

Autres remarques

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

Pictogrammes

Corrosion

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Skin Corr. 1B

Code de la classe de stockage

8A - Combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

228.2 °F - closed cup

Point d'éclair (°C)

109.0 °C - closed cup

Équipement de protection individuelle

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


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Articles

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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