C4386
Activated charcoal
acid-washed with hydrochloric acid
Synonym(s):
Charcoal activated
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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:
vapor pressure
<0.1 mmHg ( 20 °C)
Quality Level
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
≤10% moisture content
mp
3550 °C (lit.)
anion traces
chloride (Cl-): ≤0.1%
greener alternative category
, Enabling
SMILES string
[C]
InChI
1S/C
InChI key
OKTJSMMVPCPJKN-UHFFFAOYSA-N
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, acid-washed with hydrochloric acid forms a composite with natural cellulose, which can be used in the fabrication of a flexible electrode with a specific capacitance of ~103 Fg-1 for supercapacitor application. It can also be used in the preparation of ultracapacitors with asymmetric configuration.
Used in a wide variety of biochemical and immunological applications to remove reactants and waste products.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Milk Progesterone ELISA to Monitor the Success of Artificial Insemination (AI) in Buffaloes.
Kabir MS, et al.
International Journal of BioResearch, 1(3), 5-9 (2011)
Power loss and energy density of the asymmetric ultracapacitor loaded with molybdenum doped manganese oxide
Wang Y, et al.
Electrochimica Acta, 68, 95-102 (2012)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C4386-2.5KG | 04061833492079 |
| C4386-500G | 04061833492086 |