์ฝ˜ํ…์ธ ๋กœ ๊ฑด๋„ˆ๋›ฐ๊ธฐ
Merck
๋ชจ๋“  ์‚ฌ์ง„(3)

์ฃผ์š” ๋ฌธ์„œ

479411

Sigma-Aldrich

4,6-Dimethyldibenzothiophene

97%

๋™์˜์–ด(๋“ค):

4,6-DMDBT

๋กœ๊ทธ์ธ์กฐ์ง ๋ฐ ๊ณ„์•ฝ ๊ฐ€๊ฒฉ ๋ณด๊ธฐ


About This Item

์‹คํ—˜์‹(Hill ํ‘œ๊ธฐ๋ฒ•):
C14H12S
CAS Number:
Molecular Weight:
212.31
EC Number:
MDL number:
UNSPSC ์ฝ”๋“œ:
12352100
PubChem Substance ID:
NACRES:
NA.22

๋ถ„์„

97%

mp

153-157 ยฐC (lit.)

SMILES string

Cc1cccc2c3cccc(C)c3sc12

InChI

1S/C14H12S/c1-9-5-3-7-11-12-8-4-6-10(2)14(12)15-13(9)11/h3-8H,1-2H3

InChI key

MYAQZIAVOLKEGW-UHFFFAOYSA-N

์ผ๋ฐ˜ ์„ค๋ช…

4,6-Dimethyldibenzothiophene (4,6-DMDBT), a high refractory sulfur compound, is commonly found in diesel fuel. Its synthesis has been reported. The hydrodesulfurization of 4,6-DMDBT using bulk nickel alloy, bulk tungsten phosphide (WP), NiMo sulfide supported on active carbons and molecularly imprinted polymers have been reported. The dielectric behavior of 4,6-DMDBT under different microwave frequencies and temperature has been investigated.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (ยฐF)

Not applicable

Flash Point (ยฐC)

Not applicable

๊ฐœ์ธ ๋ณดํ˜ธ ์žฅ๋น„

Eyeshields, Gloves, type N95 (US)


๊ฐ€์žฅ ์ตœ์‹  ๋ฒ„์ „ ์ค‘ ํ•˜๋‚˜๋ฅผ ์„ ํƒํ•˜์„ธ์š”:

์‹œํ—˜ ์„ฑ์ ์„œ(COA)

Lot/Batch Number

์ ํ•ฉํ•œ ๋ฒ„์ „์„ ์ฐพ์„ ์ˆ˜ ์—†์œผ์‹ ๊ฐ€์š”?

ํŠน์ • ๋ฒ„์ „์ด ํ•„์š”ํ•œ ๊ฒฝ์šฐ ๋กœํŠธ ๋ฒˆํ˜ธ๋‚˜ ๋ฐฐ์น˜ ๋ฒˆํ˜ธ๋กœ ํŠน์ • ์ธ์ฆ์„œ๋ฅผ ์ฐพ์„ ์ˆ˜ ์žˆ์Šต๋‹ˆ๋‹ค.

์ด ์ œํ’ˆ์„ ์ด๋ฏธ ๊ฐ€์ง€๊ณ  ๊ณ„์‹ญ๋‹ˆ๊นŒ?

๋ฌธ์„œ ๋ผ์ด๋ธŒ๋Ÿฌ๋ฆฌ์—์„œ ์ตœ๊ทผ์— ๊ตฌ๋งคํ•œ ์ œํ’ˆ์— ๋Œ€ํ•œ ๋ฌธ์„œ๋ฅผ ์ฐพ์•„๋ณด์„ธ์š”.

๋ฌธ์„œ ๋ผ์ด๋ธŒ๋Ÿฌ๋ฆฌ ๋ฐฉ๋ฌธ

์ด๋ฏธ ์—ด๋žŒํ•œ ๊ณ ๊ฐ

Slide 1 of 6

1 of 6

Thianaphthene 95%

Sigma-Aldrich

T27405

Thianaphthene

11H-Benzo[a]carbazole

Sigma-Aldrich

UPL0003

11H-Benzo[a]carbazole

Thiophene ≥99%

Sigma-Aldrich

T31801

Thiophene

Dibenzothiophene analytical standard

Supelco

45776

Dibenzothiophene

Thiophene analytical standard

Supelco

06914

Thiophene

Dibenzothiophene for synthesis

Sigma-Aldrich

8.20409

Dibenzothiophene

Meiqin Zheng et al.
Journal of hazardous materials, 362, 424-435 (2018-09-28)
In this work, the adsorption desulfurization performance and adsorption diffusion study of B2O3 modified Ag-CeOx/TiO2-SiO2 adsorbent were investigated. The adsorption desulfurization performance was studied by batch and fixed bed tests. The homogeneous surface diffusion model (HSDM) was employed to investigate
Hussein N Nassar et al.
Environmental science and pollution research international, 28(7), 8102-8116 (2020-10-14)
One of the main precursors of air pollution and acid rains is the presence of the recalcitrant thiophenic compounds, for example dibenzothiophene (DBT) and its derivatives in transportation fuels. In an attempt to achieve the worldwide regulations of ultra-low sulfur
Hydrodesulfurization kinetics and mechanism of 4,6-dimethyldibenzothiophene over NiMo catalyst supported on carbon.
Sakanishi K, et al.
J. Mol. Catal. A: Chem., 155(1), 101-109 (2000)
Development of a novel molecularly imprinted polymer for the retention of 4,6-dimethyldibenzothiophene.
Tom LA, et al.
Microchimica Acta, 176(3-4), 375-380 (2012)
Hydrodesulfurization of dibenzothiophene, 4,6-dimethyldibenzothiophene, and their hydrogenated intermediates over bulk tungsten phosphide.
Yang L, et al.
J. Catal., 330, 330-343 (2015)

์ž์‚ฌ์˜ ๊ณผํ•™์žํŒ€์€ ์ƒ๋ช… ๊ณผํ•™, ์žฌ๋ฃŒ ๊ณผํ•™, ํ™”ํ•™ ํ•ฉ์„ฑ, ํฌ๋กœ๋งˆํ† ๊ทธ๋ž˜ํ”ผ, ๋ถ„์„ ๋ฐ ๊ธฐํƒ€ ๋งŽ์€ ์˜์—ญ์„ ํฌํ•จํ•œ ๋ชจ๋“  ๊ณผํ•™ ๋ถ„์•ผ์— ๊ฒฝํ—˜์ด ์žˆ์Šต๋‹ˆ๋‹ค..

๊ณ ๊ฐ์ง€์›ํŒ€์œผ๋กœ ์—ฐ๋ฝ๋ฐ”๋ž๋‹ˆ๋‹ค.