Chemodex

10-Acetylphenothiazine

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CDX-A0695-G0011 gCHF 116.00
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Product Details
Synonyms 10-Acetyl-10H-phenothiazine; 1-(10H-Phenothiazin-10-yl)ethanone; NSC 14724; J 3-55
Product Type Chemical
Properties
Formula C14H11NOS
MW 241.31
CAS 1628-29-1
Source/Host Chemicals Synthetic
Purity Chemicals ≥95% (NMR)
Appearance Beige powder.
Solubility Soluble in chloroform.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key DNVNQWUERFZASD-UHFFFAOYSA-N
Smiles CC(N1C2=CC=CC=C2SC3=CC=CC=C31)=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
Product Specification Sheet
Datasheet Download PDF
Description

10-Acetylphenothiazine is used as a redox shuttle additive in lithium-ion batteries (LIBs). Redox shuttles are compounds that facilitate overcharge protection by undergoing reversible redox reactions. Using 10-Acetylphenothiazine as a redox shuttle additive in lithium-ion batteries enhances their safety by providing effective overcharge protection. Its stable and reversible redox properties make it a suitable choice for this application, contributing to longer battery life and improved reliability. Can also be used as a building block or intermediate in chemical synthesis.

Product References

(1) Z. Gomurashvili & J.V. Crivello; J. Poly. Sci. Part A: Poly. Chem. 39, 1187 (2001) | (2) C. Buhrmester, et al.; J. Electrochem. Soc. 153, A288 (2006) | (3) G.P. Sarmiento, et al.; Eur. J. Med. Chem. 46, 101 (2011) | (4) J.-H. Chen, et al; J. Electrochem. Soc. 159, A1636 (2012) | (5) E. Tokunagaa & T. Okuno; Crystallogr. Commun. 68, 3369 (2012) | (6) S.A. Odom, et al.; Energy Environ. Sci. 7, 760 (2014) | (7) A.N. Matralis & A.P. Kourounakis; J. Med. Chem. 57, 2568 (2014) | (8) M.D. Casselman, et al.; Phys. Chem. Chem. Phys. 17, 6905 (2015) | (9) L. Navarro, et al.; Bioorg. Med. Chem. 26, 4113 (2018)

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