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About This Item
Empirical Formula (Hill Notation):
C
CAS Number:
Molecular Weight:
12.01
NACRES:
SB.52
PubChem Substance ID:
UNSPSC Code:
11101522
EC Number:
231-153-3
MDL number:
Product Name
Activated charcoal, untreated, granular, 20-60 mesh
InChI key
OKTJSMMVPCPJKN-UHFFFAOYSA-N
InChI
1S/C
SMILES string
[C]
vapor pressure
<0.1 mmHg ( 20 °C)
form
untreated, granular
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)
particle size
20-60 mesh
mp
3550 °C (lit.)
greener alternative category
, Enabling
Quality Level
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Application
Activated charcoal (activated carbon) has been used:
- As an adsorbent for p-cresol in the fermentation broth, during its synthesis from p-hydroxyphenylacetate catalyzed by p-hydroxyphenylacetate decarboxylase.
- To form a charcoal filter in a Drierite cartridge for removing organic compounds from the air for the odor delivery system.
- As an organic sorbent to study adsorption equilibrium of ammonia gas.
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.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Kevin C Daly et al.
PloS one, 8(11), e81863-e81863 (2013-11-28)
Sensory systems sample the external world actively, within the context of self-motion induced disturbances. Mammals sample olfactory cues within the context of respiratory cycles and have adapted to process olfactory information within the time frame of a single sniff cycle.
In-situ product recovery as a strategy to increase product yield and mitigate product toxicity.
Ng YL and Kuek YY
Open Biotechnology Journal, 7, 15-22 (2013)
Adsorption equilibria of ammonia gas on inorganic and organic sorbents at 298.15 K.
Helminen J, et al.
Journal of Chemical and Engineering Data, 46(2), 391-399 (2001)
Kohsuke Ohmatsu et al.
Nature chemistry, 6(1), 47-51 (2013-12-19)
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
Nathalie Butt et al.
Ecological applications : a publication of the Ecological Society of America, 23(4), 936-943 (2013-07-20)
A typical way to quantify aboveground carbon in forests is to measure tree diameters and use species-specific allometric equations to estimate biomass and carbon stocks. Using "citizen scientists" to collect data that are usually time-consuming and labor-intensive can play a
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