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Merck
모든 사진(2)

문서

225630

Sigma-Aldrich

Tris(2-aminoethyl)amine

96%

동의어(들):

2,2′,2′′-Nitrilotriethylamine, 2,2′,2′′-Triaminotriethylamine, TAEA

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About This Item

Linear Formula:
(NH2CH2CH2)3N
CAS Number:
Molecular Weight:
146.23
Beilstein:
1739626
EC Number:
MDL number:
UNSPSC 코드:
12162002
PubChem Substance ID:
NACRES:
NA.23

vapor density

5 (vs air)

vapor pressure

0.02 mmHg ( 20 °C)

분석

96%

형태

liquid

refractive index

n20/D 1.497 (lit.)

bp

114 °C/15 mmHg (lit.)

density

0.976 g/mL at 20 °C (lit.)

SMILES string

NCCN(CCN)CCN

InChI

1S/C6H18N4/c7-1-4-10(5-2-8)6-3-9/h1-9H2

InChI key

MBYLVOKEDDQJDY-UHFFFAOYSA-N

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관련 카테고리

일반 설명

Tris(2-aminoethyl)amine (TREN) is a water soluble tripodal ligand that is majorly used in co-ordination chemistry. It has three aminoethylgroups that attach with the surface atoms to provide a scaffold assembly.

애플리케이션

Building block for cryptands; precursor to a proazaphosphatrane, a stong, nonionic base.
TREN can be grafted with multi-walled carbon nanotube (MWCNT) for use in solid phase extraction of metal ions for wastewater treatment based applications. It can also be used as a chelating agent in the surface treatment of silica nanoparticles which can further be used for a wide range of industrial applications.

픽토그램

Skull and crossbonesCorrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 3 Oral - Skin Corr. 1B

Storage Class Code

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

WGK

WGK 3

Flash Point (°F)

235.4 °F - closed cup

Flash Point (°C)

113 °C - closed cup

개인 보호 장비

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

Surface treatment of silica nanoparticles for stable and charge-controlled colloidal silica
Kim K, et al.
International journal of nanomedicine, 9(2), 29-29 (2014)
Removal of lead ions from wastewater using functionalized multiwalled carbon nanotubes with tris (2-aminoethyl) amine
Tehrani MS, et al.
Journal of Environmental Protection, 4(06), 529-529 (2013)
Polish Journal of Chemistry, 80, 1825-1825 (2006)
Chinta Reddy Venkat Reddy et al.
The Journal of organic chemistry, 72(8), 3093-3096 (2007-03-21)
1,4-additions to a variety of Michael acceptors with a wide variety of donors were efficiently catalyzed at room temperature by the title reusable Merrifield resin-supported catalyst. Advantages of this catalyst include a simple workup (filtration of the reaction mixture) and
Sulfate recognition by persistent crystalline capsules with rigidified hydrogen-bonding cavities.
Radu Custelcean et al.
Angewandte Chemie (International ed. in English), 47(10), 1866-1870 (2008-02-01)

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