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344621

Sigma-Aldrich

Sulfur

flakes, ≥99.99% trace metals basis

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About This Item

Empirical Formula (Hill Notation):
S
CAS Number:
7704-34-9
Molecular Weight:
32.07
EC Number:
231-722-6
MDL number:
MFCD00085316
UNSPSC Code:
12141912
PubChem Substance ID:
24861269
NACRES:
NA.23

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

SMILES string

[S]

InChI

1S/S

InChI key

NINIDFKCEFEMDL-UHFFFAOYSA-N

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315

Hazard Classifications

Skin Irrit. 2

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
William Tam et al.
Journal of molecular biology, 425(14), 2450-2462 (2013-04-02)
The assembly of long non-contractile phage tails begins with the formation of the tail tip complex (TTC). TTCs are multi-functional protein structures that mediate host cell adsorption and genome injection. The TTC of phage λ is assembled from multiple copies
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
Chemoselective peptide ligation-desulfurization at aspartate.
Robert E Thompson et al.
Angewandte Chemie (International ed. in English), 52(37), 9723-9727 (2013-07-31)
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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