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Sigma-Aldrich

4-tert-Butylbenzenethiol

97%

Synonym(s):

4-tert-Butylthiophenol

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About This Item

Linear Formula:
(CH3)3CC6H4SH
CAS Number:
2396-68-1
Molecular Weight:
166.28
EC Number:
219-255-6
MDL number:
MFCD00022067
UNSPSC Code:
12352100
PubChem Substance ID:
24881461
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.5480 (lit.)

bp

238 °C (lit.)

density

0.964 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)c1ccc(S)cc1

InChI

1S/C10H14S/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7,11H,1-3H3

InChI key

GNXBFFHXJDZGEK-UHFFFAOYSA-N

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Application

4-tert-Butylbenzenethiol can be used to synthesize Pd–thiolate complex by coordinating with Pd2+.The reduction of this complex forms ultrasmall palladium nanoclusters.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

>230.0 °F - closed cup

flash_point_c

> 110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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Gaya N Andrew et al.
Chemistry, an Asian journal, 15(23), 4077-4081 (2020-10-14)
We report the single-crystal synthesis of a chlorine-centered bimetallic cluster, Cl@Ag22 Au6 (4-TBBT)28 (PPh4 ), which bears a quatrefoil-structured Cl@Ag22 (SR)16 core studded by six Au(SR)2 staples showing a quasi Td symmetry. This cluster bears 28 metal atoms and 28
Yongbo Song et al.
Nature communications, 11(1), 478-478 (2020-01-26)
Gold-copper alloys have rich forms. Here we report an atomically resolved [Au52Cu72(p-MBT)55]+Cl- nanoalloy (p-MBT = SPh-p-CH3). This nanoalloy exhibits unusual structural patterns. First, two Cu atoms are located in the inner 7-atom decahedral kernel (M7, M = Au/Cu). The M7 kernel is then enclosed
Masaaki Yusa et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 16(7), 1043-1048 (2017-05-10)
Under the irradiation of red light (690 nm), quinones were converted to hydroquinones by thiols in the presence of metallophthalocyanines. The reaction proceeded via the charge separation between the triplet state of phthalocyanine and the quinone. The product determining step

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