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292753

Sigma-Aldrich

Pentaethylenehexamine

technical grade

Synonym(s):

3,6,9,12-Tetraazatetradecane-1,14-diamine

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About This Item

Linear Formula:
NH2CH2CH2NH(CH2CH2NH)3CH2CH2NH2
CAS Number:
4067-16-7
Molecular Weight:
232.37
Beilstein:
1768042
EC Number:
223-775-9
MDL number:
MFCD00008167
UNSPSC Code:
12352100
PubChem Substance ID:
24857609
NACRES:
NA.22

grade

technical grade

refractive index

n20/D 1.5096 (lit.)

solubility

water: soluble 500 g/L at 20 °C

density

0.95 g/mL at 25 °C (lit.)

SMILES string

NCCNCCNCCNCCNCCN

InChI

1S/C10H28N6/c11-1-3-13-5-7-15-9-10-16-8-6-14-4-2-12/h13-16H,1-12H2

InChI key

LSHROXHEILXKHM-UHFFFAOYSA-N

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General description

Pentaethylenehexamine (PEHA) is an acyclic polyamine that can be used to prepare amine-modified adsorbent.

Application

5.Pentaethylenehexamine has been used in the preparation of:
  • polyisobutylene succinimide (PIBSI) dispersants, used as engine oil-additives
  • poly(glycidyl methacrylate) (P(GMA)) homopolymers
  • poly(amidoamine)s

Signal Word

Danger

Hazard Statements

H314,H317,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Pentaethylenehexamine loaded SBA-16 for CO2 capture from simulated flue gas
Liu Y, et al.
Powder Technology, 318, 186-192 (2017)
Gunniya Hariyanandam Gunasekar et al.
Inorganic chemistry, 58(6), 3717-3723 (2019-03-02)
Today, one of the most imperative targets to realize the conversions of CO2 in industry is the development of practically viable catalytic systems that demonstrate excellent activity, selectivity, and durability. Herein, a simple heterogeneous Ru(III) catalyst is prepared by immobilizing
Gas-phase H/D exchange reactions of polyamine complexes:(M+ H)+,(M+ alkali metal+), and (M+ 2H) 2+
Reyzer ML and Brodbelt JS
Journal of the American Society For Mass Spectrometry, 11, 711-721 (2000)
Solmaz Pirouz et al.
The journal of physical chemistry. B, 118(14), 3899-3911 (2014-03-19)
A novel methodology based on fluorescence quenching measurements is introduced to determine quantitatively the amine content of polyisobutylene succinimide (PIBSI) dispersants used as engine oil-additives. To this end, a series of five PIBSI dispersants were prepared by reacting 2 mol
Lisa E Prevette et al.
Biomacromolecules, 11(2), 326-332 (2010-01-12)
Previously, a series of three poly(amidoamine)s was designed and synthesized by polymerizing oxylate, succinate, or adipate groups with pentaethylenehexamine. These resulting polymers (named O4, S4, and A4, respectively) were created as models to poly(glycoamidoamine) nucleic acid delivery agents to understand
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