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Merck

344621

Sulfur

flakes, ≥99.99% trace metals basis

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About This Item

Empirical Formula (Hill Notation):
S
CAS Number:
Molecular Weight:
32.07
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12141912
EC Number:
231-722-6
MDL number:
assay:
≥99.99% trace metals basis
form:
flakes

Product Name

Sulfur, flakes, ≥99.99% trace metals basis

InChI key

NINIDFKCEFEMDL-UHFFFAOYSA-N

InChI

1S/S

SMILES string

[S]

vapor density

8.9 (vs air)

vapor pressure

1 mmHg ( 183.8 °C)
10 mmHg ( 246 °C)

assay

≥99.99% trace metals basis

form

flakes

autoignition temp.

450 °F
450 °F

resistivity

2E23 μΩ-cm, 20°C

bp

444.7 °C (lit.)

mp

112.8 °C (rhombic) (lit.)
117-120 °C (lit.)
119.0 °C (monoclinic) (lit.)

density

2.07 g/mL at 25 °C

Quality Level

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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Irrit. 2

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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Jubok Lee et al.
Nano letters, 21(1), 43-50 (2020-10-15)
The extreme elastic strain of monolayer transition metal dichalcogenides provides an ideal platform to achieve efficient exciton funneling via local strain modulation; however, studies conducted thus far have focused on the use of substrates with fixed strain profiles. We prepared
Farhad Forouhar et al.
Nature chemical biology, 9(5), 333-338 (2013-04-02)
How living organisms create carbon-sulfur bonds during the biosynthesis of critical sulfur-containing compounds is still poorly understood. The methylthiotransferases MiaB and RimO catalyze sulfur insertion into tRNAs and ribosomal protein S12, respectively. Both belong to a subgroup of radical-S-adenosylmethionine (radical-SAM)
Chemoselective peptide ligation-desulfurization at aspartate.
Robert E Thompson et al.
Angewandte Chemie (International ed. in English), 52(37), 9723-9727 (2013-07-31)
Yu Kobayashi et al.
ACS nano, 9(4), 4056-4063 (2015-03-27)
Atomic-layer transition metal dichalcogenides (TMDCs) have attracted appreciable interest due to their tunable band gap, spin-valley physics, and potential device applications. However, the quality of TMDC samples available still poses serious problems, such as inhomogeneous lattice strain, charge doping, and
Gulluzar Bastug et al.
The Journal of organic chemistry, 78(18), 9303-9308 (2013-08-14)
The newly prepared complex [Pd(IPr*(OMe))(cin)(Cl)] provides high catalytic activity for carbon-sulfur cross-coupling reactions. Nonactivated and deactivated aryl halides were successfully coupled with a large variety of aryl- and alkylthiols using this well-defined palladium N-heterocyclic carbene (NHC) complex.

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