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Merck
CN

421960

Bis(hexamethylene)triamine

high purity

Synonym(s):

6,6′-Iminodihexylamine, Bis(6-aminohexyl)amine

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About This Item

Linear Formula:
NH2(CH2)6NH(CH2)6NH2
CAS Number:
Molecular Weight:
215.38
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-593-1
Beilstein/REAXYS Number:
2323517
MDL number:
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InChI key

MRNZSTMRDWRNNR-UHFFFAOYSA-N

InChI

1S/C12H29N3/c13-9-5-1-3-7-11-15-12-8-4-2-6-10-14/h15H,1-14H2

SMILES string

NCCCCCCNCCCCCCN

vapor pressure

<0.01 mmHg ( 25 °C)

form

solid

refractive index

n20/D 1.49 (lit.)

bp

163-165 °C/4 mmHg (lit.)

mp

33-36 °C (lit.)

density

0.85 g/mL at 20 °C (lit.), 0.879 g/mL at 25 °C

General description

Bis(hexamethylene)triamine (Bis-HEA, BHMT, BHMTA) is an aliphatic polyamine. It is a spermidine analog and has been reported to lack the enhancing effect on mitochondrial Ca(2+) accumulation but shows inhibitory effect on the Ca(2+) and Pi-induced mitochondrial permeability transition. Its ability in inhibiting shale swelling and dispersion in water-based drilling fluid has been investigated.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Interior synthesizing of ZnO nanoflakes inside nylon-6 electrospun nanofibers.
Panthi G, et al.
Journal of Applied Polymer Science, 127(3), 2025-2032 (2013)
Co3O4-ZnO hierarchical nanostructures by electrospinning and hydrothermal methods.
Kanjwal MA, et al.
Applied Surface Science, 257(18), 7975-7981 (2011)
Antibacterial and photocatalytic properties of Ag/TiO2/ZnO nano-flowers prepared by facile one-pot hydrothermal process.
Pant HR, et al.
Ceramics International, 39(2), 1503-1510 (2013)
Bis (hexamethylene) triamine as potential shale inhibitor in water-based drilling fluid.
Zhong H, et al.
Open Petroleum Engineering Journal, 6, 49-56 (2013)
Laurence Covassin et al.
Bioorganic & medicinal chemistry letters, 13(19), 3267-3271 (2003-09-03)
Dimeric norspermidine and spermidine derivatives are strong competitive inhibitors of polyamine transport. A xylyl tether was used for the dimerization of various triamines and spermine via a secondary amino group, and of putrescine via an ether or an amino group.

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