9H-Thioxanthen-9-one, 4-(1-methylethyl)-


Chemical Name: 9H-Thioxanthen-9-one, 4-(1-methylethyl)-
CAS Number: 83846-86-0
Product Number: AG004S5Y(AGN-PC-0JPLS8)
Synonyms:
MDL No:
Molecular Formula: C16H14OS
Molecular Weight: 254.3468

Identification/Properties


Properties
MP:
107-109°C
BP:
391.0±32.0 °C(Predicted)
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
254.347g/mol
XLogP3:
4.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
254.077g/mol
Monoisotopic Mass:
254.077g/mol
Topological Polar Surface Area:
42.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
325
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



4-Isopropylthioxanthone, also known as IP-TX, is a versatile compound widely used in chemical synthesis for its photoinitiating properties. This molecule plays a crucial role in initiating photopolymerization reactions, where exposure to ultraviolet (UV) light triggers the decomposition of 4-Isopropylthioxanthone into reactive radicals. These radicals then initiate polymerization processes in various applications, such as in the production of coatings, adhesives, inks, and photoresists. Additionally, 4-Isopropylthioxanthone is valued for its ability to efficiently crosslink polymers under UV irradiation, leading to the formation of high-performance, durable materials. In summary, 4-Isopropylthioxanthone serves as a key component in the realm of chemical synthesis, facilitating the production of advanced materials with enhanced properties.