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Safety Information

132071

Sigma-Aldrich

1,3,5-Triethylbenzene

≥97%

Synonym(s):

1,3,5-Triethylbenzene

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About This Item

Linear Formula:
C6H3(C2H5)3
CAS Number:
Molecular Weight:
162.27
Beilstein:
2039481
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥97%

form

liquid

refractive index

n20/D 1.495 (lit.)

bp

215 °C (lit.)

density

0.862 g/mL at 25 °C (lit.)

SMILES string

CCc1cc(CC)cc(CC)c1

InChI

1S/C12H18/c1-4-10-7-11(5-2)9-12(6-3)8-10/h7-9H,4-6H2,1-3H3

InChI key

WJYMPXJVHNDZHD-UHFFFAOYSA-N

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Application

1,3,5-Triethylbenzene was used as a supramoelcular template to organize molecular-recognition elements. It was also used to synthesize a series of di- and trinucleating ligands.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

168.8 °F - closed cup

Flash Point(C)

76 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

132071-BULK:
132071-5G:
132071-50G:
132071-VAR:
132071-25G:
132071-10G:


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Gou Higashihara et al.
Dalton transactions (Cambridge, England : 2003), (14)(14), 1888-1898 (2008-03-29)
A series of di- and trinucleating ligands with a 1,3,5-triethylbenzene core connected to N,N-bidentate tethers was synthesized. The ligands readily reacted with monuclear Rh and Pd precursors to give the corresponding di- and trinuclear complexes, which were characterized by using
Xing Wang et al.
Beilstein journal of organic chemistry, 8, 1-10 (2012-03-17)
1,3,5-triethylbenzenes have been widely used as supramolecular templates to organize molecular-recognition elements. It is believed that the steric-gearing effect of the 1,3,5-triethylbenzene template directs the binding elements toward the same face of the central ring, hence increasing the binding affinity.

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