Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

View All Documentation

308102

Sigma-Aldrich

N,N-Dimethylhexylamine

98%

Synonym(s):

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

Sign Into View Organizational & Contract Pricing

Select a Size

5 G
$59.70
25 G
$231.00

$59.70

In StockDetails

Request a Bulk Order
All Photos(2)

Select a Size

Change View
5 G
$59.70
25 G
$231.00

About This Item

Linear Formula:
CH3(CH2)4CH2N(CH3)2
CAS Number:
4385-04-0
Molecular Weight:
129.24
Beilstein/REAXYS Number:
1732757
EC Number:
224-491-8
MDL number:
MFCD00009522
UNSPSC Code:
12352100
PubChem Substance ID:
24858648
NACRES:
NA.22
form:
liquid
assay:
98%

$59.70

In StockDetails

Request a Bulk Order

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

Looking for similar products? Visit Product Comparison Guide

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[1].

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[2]. 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[3].

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000396506
0000397779
0000396507
0000335396
0000387569

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

N,N-Dimethylethylamine ≥99%

Sigma-Aldrich

652571

N,N-Dimethylethylamine

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)
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
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

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service