28-5860
Sulfur
SAJ first grade, ≥98.0%
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About This Item
Empirical Formula (Hill Notation):
S
CAS Number:
Molecular Weight:
32.07
UNSPSC Code:
12141912
PubChem Substance ID:
MDL number:
Assay:
≥98.0%
Grade:
SAJ first grade
Form:
solid
InChI
1S/S
SMILES string
[S]
InChI key
NINIDFKCEFEMDL-UHFFFAOYSA-N
grade
SAJ first grade
vapor density
8.9 (vs air)
vapor pressure
1 mmHg ( 183.8 °C), 10 mmHg ( 246 °C)
assay
≥98.0%
form
solid
availability
available only in Japan
resistivity
2E23 μΩ-cm, 20°C
bp
444.7 °C (lit.)
mp
112.8 °C (rhombic) (lit.), 119.0 °C (monoclinic) (lit.)
storage temp.
15-25°C
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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
Regulatory Information
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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
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)
Kuan-Yeow Show et al.
Biotechnology advances, 31(4), 409-420 (2012-12-27)
Biological removal of carbon, nitrogen and sulfur is drawing increasing research interest in search for an efficient and cost-effective wastewater treatment. While extensive work on separate removal of nitrogen and sulfur is well documented, investigation on simultaneous denitrifying sulfide removal
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.
Chemoselective peptide ligation-desulfurization at aspartate.
Robert E Thompson et al.
Angewandte Chemie (International ed. in English), 52(37), 9723-9727 (2013-07-31)
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