Skip to Content
Merck
CN

Key Documents

View All Documentation

223778

1,3,5-Tri-tert-butylbenzene

97%

Synonym(s):

1,3,5-Tri-t-butylbenzene, 1,3,5-Tris(1,1-dimethylethyl)benzene, 1,3,5-Tris(tert-butyl)benzene, 1,3,5-Tritert-butylbenzene

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
C6H3[C(CH3)3]3
CAS Number:
1460-02-2
Molecular Weight:
246.43
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24853403
EC Number:
215-952-4
Beilstein/REAXYS Number:
1909579
MDL number:
MFCD00008831
Assay:
97%
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

200

assay

97%

form

solid

bp

121-122 °C/12 mmHg (lit.)

mp

67-72 °C (lit.)

SMILES string

CC(C)(C)c1cc(cc(c1)C(C)(C)C)C(C)(C)C

InChI

1S/C18H30/c1-16(2,3)13-10-14(17(4,5)6)12-15(11-13)18(7,8)9/h10-12H,1-9H3

InChI key

GUFMBISUSZUUCB-UHFFFAOYSA-N

General description

The Sandros-Boltzmann (SB) dependency on the reaction free energy of 1,3,5-tri-tert-butylbenzene has been studied.

Still not finding the right product?

Explore all of our products under 1,3,5-Tri-tert-butylbenzene

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BGBC5194V
BGBC3123V
BGBC1990V
BGBC1989V
BGBC1988V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Lingling Liu et al.
Journal of oleo science, 66(9), 981-990 (2017-08-11)
An offline solid-phase extraction (SPE) approach combined with a large-volume injection (LVI)-gas chromatography-flame ionization detector (LVI-GC-FID) is improved for routine analysis of mineral oil saturated hydrocarbons (MOSH) in vegetable oils. The key procedure of the method consists in using offline
Yaoqing Xie et al.
Food chemistry, 294, 458-467 (2019-05-28)
On-line high-performance liquid chromatography coupled with gas chromatography with flame ionization detector (LC-GC) has become an important technique for the determination of mineral oil aromatic hydrocarbons (MOAH) in foods. However, the analysis is complicated and time-consuming. The present study aimed
Roccaldo Sardella et al.
Chirality, 29(9), 536-540 (2017-07-06)
The capacity of nonsteroidal antiinflammatory drugs (NSAIDs) to prevent prostanoids biosynthesis through the inhibition of COX-2 enzyme is related to their structural backbone, based on the fusion of a cis-stilbene unit with a variety of heterocyclic and carbocyclic rings. By
View All Related Papers

Global Trade Item Number

SKUGTIN
223778-50G04061833063507
223778-10G04061833063491