Skip to Content
Merck
CN

28-5860

Sulfur

SAJ first grade, ≥98.0%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

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
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


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

autoignition temp.

450 °F

availability

available only in Japan

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.)

storage temp.

15-25°C

SMILES string

[S]

InChI

1S/S

InChI key

NINIDFKCEFEMDL-UHFFFAOYSA-N



Still not finding the right product?

Explore all of our products under Sulfur


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

Regulatory Information

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



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)
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.