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Sigma-Aldrich

N,N-Dimethylbutylamine

99%

Synonyme(s) :

N-Butyldimethylamine

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About This Item

Formule linéaire :
CH3(CH2)3N(CH3)2
Numéro CAS:
927-62-8
Poids moléculaire :
101.19
Numéro Beilstein :
1731308
Numéro CE :
213-156-1
Numéro MDL:
MFCD00043838
Code UNSPSC :
12352100
ID de substance PubChem :
24862984

Pureté

99%

Indice de réfraction

n20/D 1.398 (lit.)

Point d'ébullition

93.3 °C/750 mmHg (lit.)

Densité

0.721 g/mL at 25 °C (lit.)

Chaîne SMILES 

CCCCN(C)C

InChI

1S/C6H15N/c1-4-5-6-7(2)3/h4-6H2,1-3H3

Clé InChI

DJEQZVQFEPKLOY-UHFFFAOYSA-N

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Description générale

N,N-Dimethylbutylamine is a tertiaryalkylamine. X-ray photoelectron spectra (XPS) of Si(001) surfaces exposed to N,N-dimethylbutylamine at 300K has been reported.

Application

N,N-Dimethylbutylamine is suitable for use in the fabrication of polystyrene-based nano-LC monolithic columns for the separation of protein molecules. It may be used as ion-pairing reagent in a study involving comparison of performance of six ion-pairing reagents as mobile phase modifiers for oligonucleotide LC/MS.

Pictogrammes

FlameSkull and crossbonesCorrosion
GHS02,GHS06,GHS05

Mention d'avertissement

Danger

Mentions de danger

H225,H301,H314,H335

Classification des risques

Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

23.0 °F - closed cup

Point d'éclair (°C)

-5 °C - closed cup

Équipement de protection individuelle

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

Certificats d'analyse (COA)

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Leta Deressa Tolesa et al.
International journal of biological macromolecules, 130, 818-826 (2019-03-07)
Ammonium-based ionic liquids (ILs): diisopropylethylammonium acetate ([DIPEA][Ac]), diisopropylethylammonium propanoate ([DIPEA][P]) and dimethylbutylammonium acetate ([DMBA][Ac]) are used for the extraction of chitin from shrimp shells. The extracted chitins were characterized by FT-IR, TGA, XRD, SEM and 1H NMR. The yield of
Lingzhi Gong et al.
Rapid communications in mass spectrometry : RCM, 28(4), 339-350 (2014-01-08)
A sensitive and selective liquid chromatography/mass spectrometry (LC/MS) method is essential for quality control of synthetic oligonucleotides. However, researchers are still searching for improvements to ion-pairing reagents for ion-pairing reversed-phase LC/MS. This study performed a comprehensive comparison of six ion-pairing
Anna Kilanowska et al.
Analytical and bioanalytical chemistry, 412(27), 7453-7467 (2020-08-29)
The aim of the present investigation was the analysis and identification of antisense oligonucleotide metabolism products after incubation with human liver microsomes regarding four different oligonucleotide modifications. Separation and detection methods based on the use of liquid chromatography coupled with
Łukasz Nuckowski et al.
The Analyst, 144(15), 4622-4632 (2019-06-28)
Our research focused on applying microextraction by packed sorbent to extracting antisense oligonucleotides from serum samples. The tested sorbents included poly(styrene-co-divinylbenzene), octyl, octadecyl, and unmodified silica gel. As nonpolar sorbents were used for highly-polar molecules, this required ion-pair mode. Comprehensive
Sylwia Studzińska et al.
Analytical and bioanalytical chemistry, 408(6), 1585-1595 (2016-01-14)
Ultra high performance liquid chromatography hyphenated with quadrupole time-of-flight mass spectrometry was used to determine the products of the in vitro metabolism of phosphorothioate oligonucleotides. These compounds may be used during antisense therapy as synthetic fragments of genes. For this
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