369527
N,N-Dimethylbutylamine
99%
Synonym(s):
N-Butyldimethylamine
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About This Item
Linear Formula:
CH3(CH2)3N(CH3)2
CAS Number:
Molecular Weight:
101.19
EC Number:
213-156-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1731308
MDL number:
InChI key
DJEQZVQFEPKLOY-UHFFFAOYSA-N
InChI
1S/C6H15N/c1-4-5-6-7(2)3/h4-6H2,1-3H3
SMILES string
CCCCN(C)C
assay
99%
bp
93.3 °C/750 mmHg (lit.)
density
0.721 g/mL at 25 °C (lit.)
General description
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.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
23.0 °F - closed cup
flash_point_c
-5 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Joshua E S J Reid et al.
Physical chemistry chemical physics : PCCP, 19(41), 28133-28138 (2017-10-13)
The ionic nature of a functionalized protic ionic liquid cannot be rationalized simply through the differences in aqueous proton dissociation constants between the acid precursor and the conjugate acid of the base precursor. The extent of proton transfer, i.e. the
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
Anna Kilanowska et al.
Journal of chromatography. A, 1622, 461100-461100 (2020-05-04)
The aim of the present investigation was application of hydrophilic interaction liquid chromatography as an alternative chromatographic approach for the study of antisense oligonucleotides. The influence of several mobile phases, differing with the salt type, their concentration and pH value
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
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
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