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369527

Sigma-Aldrich

N,N-Dimethylbutylamine

99%

Synonym(s):

N-Butyldimethylamine

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About This Item

Linear Formula:
CH3(CH2)3N(CH3)2
CAS Number:
927-62-8
Molecular Weight:
101.19
Beilstein/REAXYS Number:
1731308
EC Number:
213-156-1
MDL number:
MFCD00043838
UNSPSC Code:
12352100
PubChem Substance ID:
24862984

assay

99%

refractive index

n20/D 1.398 (lit.)

bp

93.3 °C/750 mmHg (lit.)

density

0.721 g/mL at 25 °C (lit.)

SMILES string

CCCCN(C)C

InChI

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

InChI key

DJEQZVQFEPKLOY-UHFFFAOYSA-N

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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.[1]

Application

N,N-Dimethylbutylamine is suitable for use in the fabrication of polystyrene-based nano-LC monolithic columns for the separation of protein molecules.[2] 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.[3]

signalword

Danger

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_germany

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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Certificates of Analysis (COA)

Lot/Batch Number
BCBK4703V
BCBM6134V
BCBF9443V
BCBF5572V
1436172V

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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
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
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
Cristina Legido-Quigley et al.
Journal of chromatography. A, 1030(1-2), 195-200 (2004-03-27)
This report details the fabrication of polystyrene-based nano-LC monolithic columns for the separation of protein molecules. The report focuses on the practical advantages of monolithic columns when compared to conventional packed columns. Capillary columns were made to 100 and 50
Camille Samson et al.
Biomolecules, 10(12) (2020-12-12)
Archaeal DNA polymerases from the B-family (polB) have found essential applications in biotechnology. In addition, some of their variants can accept a wide range of modified nucleotides or xenobiotic nucleotides, such as 1,5-anhydrohexitol nucleic acid (HNA), which has the unique
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