Skip to Content
Merck
CN

131202

Dihexylamine

97%

Synonym(s):

Bis(1-hexyl)amine

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
[CH3(CH2)5]2NH
CAS Number:
143-16-8
Molecular Weight:
185.35
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848001
EC Number:
205-588-4
Beilstein/REAXYS Number:
1738519
MDL number:
MFCD00009521

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Dihexylamine, 97%

InChI key

PXSXRABJBXYMFT-UHFFFAOYSA-N

InChI

1S/C12H27N/c1-3-5-7-9-11-13-12-10-8-6-4-2/h13H,3-12H2,1-2H3

SMILES string

CCCCCCNCCCCCC

vapor density

6.4 (vs air)

assay

97%

form

liquid

refractive index

n20/D 1.432 (lit.)

bp

192-195 °C (lit.)

density

0.795 g/mL at 25 °C (lit.)

functional group

amine

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Dihexylamine was used in the preparation of succinic acid.

General description

Dihexylamine nitrosation rate was enhanced when the reaction was carried out in the presence of micelles containing bile acid conjugates and lecithin.

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1A

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 2

flash_point_f

203.0 °F - closed cup

flash_point_c

95 °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
SDBB4812
STBL1772
STBL3155
S77817
STBB1338V

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

Y K Kim et al.
IARC scientific publications, (31)(31), 207-214 (1980-01-01)
The rate of nitrosation of dihexylamine is enhanced when the reaction is carried ut in the presence of micelles containing bile acid conjugates or bile acid conjugates and lecithin. The nitrosation of smaller dialkylamines is not affected. The nitrosation of
Tanja Kurzrock et al.
Bioprocess and biosystems engineering, 34(7), 779-787 (2011-02-26)
Biotechnologically produced succinic acid has the potential to displace maleic acid and its uses and to become an important feedstock for the chemical industry. In addition to optimized production strains and fermentation processes, an efficient separation of succinic acid from

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