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Key Documents

131202

Sigma-Aldrich

Dihexylamine

97%

Synonym(s):

Bis(1-hexyl)amine

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About This Item

Linear Formula:
[CH3(CH2)5]2NH
CAS Number:
Molecular Weight:
185.35
Beilstein/REAXYS Number:
1738519
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

6.4 (vs air)

Quality Level

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

SMILES string

CCCCCCNCCCCCC

InChI

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

InChI key

PXSXRABJBXYMFT-UHFFFAOYSA-N

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General description

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

Application

Dihexylamine was used in the preparation of succinic acid.

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_germany

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


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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

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