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308102

Sigma-Aldrich

N,N-Dimethylhexylamine

98%

Sinónimos:

1-(Dimethylamino)hexane, N,N-Dimethyl-1-hexanamine, N,N-Dimethyl-n-hexylamine, N,N-Dimethylhexylamine, N-Hexyldimethylamine

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About This Item

Fórmula lineal:
CH3(CH2)4CH2N(CH3)2
Número de CAS:
4385-04-0
Peso molecular:
129.24
Beilstein/REAXYS Number:
1732757
EC Number:
224-491-8
MDL number:
MFCD00009522
UNSPSC Code:
12352100
PubChem Substance ID:
24858648
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.414 (lit.)

bp

146-150 °C (lit.)

density

0.744 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCCCCCN(C)C

InChI

1S/C8H19N/c1-4-5-6-7-8-9(2)3/h4-8H2,1-3H3

InChI key

QMHNQZGXPNCMCO-UHFFFAOYSA-N

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General description

The free Salinomycin (Sali), that has selective toxicity to cancer stem cells (CSCs), was encapsulated into the nanoparticle along with the additive N,N-dimethylhexylamine.

Application

N,N-Dimethylhexylamine was used as ion-pairing agent to study the problem of poor retention of uridine diphosphate-linked intermediates on reverse phase media. It was also used in the determining the five monophosphate nucleotides (cytidine 5′-monophosphate, uridine 5′-monophosphate, adenosine 5′-monophosphate, inosine 5′-monophosphate and guanosine 5′-monophosphate) in baby foods.

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H314

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

93.2 °F - closed cup

flash_point_c

34 °C - closed cup

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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N,N-Dimethylethylamine ≥99%

Sigma-Aldrich

652571

N,N-Dimethylethylamine

Pilar Viñas et al.
Journal of chromatography. A, 1217(32), 5197-5203 (2010-06-29)
A liquid chromatography with diode array detection coupled to dual electrospray atmospheric pressure chemical ionization time-of-flight mass spectrometry (HPLC/ESI-APCI-TOF-MS) method is described for the rapid determination of five monophosphate nucleotides (cytidine 5'-monophosphate, uridine 5'-monophosphate, adenosine 5'-monophosphate, inosine 5'-monophosphate and guanosine
Peng Zhao et al.
Molecular pharmaceutics, 11(8), 2703-2712 (2014-06-25)
Salinomycin (Sali) has selective toxicity to cancer stem cells (CSCs), a subpopulation of cancer cells that have been recently linked with tumor multidrug resistance (MDR). To utilize its selective toxicity for cancer therapy, we sought to devise a nanoparticle (NP)
Harika Vemula et al.
Analytical biochemistry, 465, 12-19 (2014-08-03)
Bacterial cell wall biosynthesis is the target of several antibiotics and is of interest as a target for new inhibitor development. The cytoplasmic steps of this pathway involve a series of uridine diphosphate (UDP)-linked peptidoglycan intermediates. Quantification of these intermediates

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