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C5510

Sigma-Aldrich

Activated charcoal

greener alternative

acid-washed with phosphoric and sulfuric acids

Synonym(s):

Charcoal activated

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About This Item

Empirical Formula (Hill Notation):
C
CAS Number:
7440-44-0
Molecular Weight:
12.01
EC Number:
231-153-3
MDL number:
MFCD00133992
UNSPSC Code:
23201100
PubChem Substance ID:
329775088
NACRES:
SB.52

vapor pressure

<0.1 mmHg ( 20 °C)

Quality Level

100

form

powder

autoignition temp.

842 °F

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

resistivity

1375 μΩ-cm, 20°C (graphite)

impurities

≤1.0% acid solubles
≤10% moisture content

mp

3550 °C (lit.)

greener alternative category

Enabling,

SMILES string

[C]

InChI

1S/C

InChI key

OKTJSMMVPCPJKN-UHFFFAOYSA-N

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General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Click here for more details.

Application

Activated charcoal was used to adsorb lignin and hemicelluloses in spent liquor from neutral sulfite semichemical (NSSC) pulping process.

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Mehdi Dashtban et al.
Journal of environmental management, 136, 62-67 (2014-02-26)
Hemicelluloses and lignin present in the spent liquor (SL) of neutral sulfite semichemical (NSSC) pulping process can potentially be converted into value-added products such as furfural, hydroxymethylfurfural, levulinic acid, phenols and adhesives. However, the direct conversion of hemicelluloses and lignin
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The development of a general catalytic method for the direct and stereoselective construction of contiguous all-carbon quaternary stereocentres remains a formidable challenge in chemical synthesis. Here, we report a highly enantio- and diastereoselective [3+2] annulation reaction of 5-vinyloxazolidinones and activated
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