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2-Isopropylthioxanthone

PESTANAL®, analytical standard

Synonyme(s) :

2-Isopropyl-9H-thioxanthen-9-one

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About This Item

Formule empirique (notation de Hill):
C16H14OS
Numéro CAS:
5495-84-1
Poids moléculaire :
254.35
Numéro CE :
226-827-9
Numéro MDL:
MFCD00055658
Code UNSPSC :
41116107
ID de substance PubChem :
329754906
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

environmental

Format

neat

Chaîne SMILES 

CC(C)c1ccc2Sc3ccccc3C(=O)c2c1

InChI

1S/C16H14OS/c1-10(2)11-7-8-15-13(9-11)16(17)12-5-3-4-6-14(12)18-15/h3-10H,1-2H3

Clé InChI

KTALPKYXQZGAEG-UHFFFAOYSA-N

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Description générale

2-Isopropylthioxanthone is a compound, which can play the role of a sulfur type photoinitiator in printing industries and UV-cured inks for food packaging materials.

Application

2-Isopropylthioxanthone has been used as an analytical standard for the determination of the analyte in packaged food materials using liquid chromatography-tandem mass spectrometry (LC–MS/MS). It may be used as an analytical standard for the determination of the analyte in milk, fruit drinks and packaged beverages by high performance liquid chromatography (HPLC) coupled to MS/MS and micellar electrokinetic chromatography techniques (MEKC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Informations légales

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictogrammes

Health hazardEnvironment
GHS08,GHS09

Mention d'avertissement

Warning

Mentions de danger

H361f,H410

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
BCCK2348
BCBX4608
SZBD234XV
SZBC065XV
SZB9105XV

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Xiaotian Zhao et al.
Journal of molecular modeling, 26(3), 56-56 (2020-02-13)
The activation or functionalization of the saturated C-H is an extremely active field at present. We have explored the triplet state thioxanthone in reactivity of the hydrogen transfer reaction between donors and acceptors. In our works, two donors with quasi-inert
Direct analysis of isopropylthioxanthone (ITX) in milk by high?performance liquid chromatography/tandem mass spectrometry
Bagnati R, et al.
Rapid Communications in Mass Spectrometry, 21, 1998-2002 (2007)
Ye Fan et al.
Colloids and surfaces. B, Biointerfaces, 167, 385-391 (2018-04-28)
FAVs (fatty acid vesicles), originated from natural biomass and created available biointerface, have advantages of biocompatibility, low-cost, and easy self-assembly in aqueous solution due to their dynamic feature. However, there is no example of applying FAVs in contact with human
AhR-agonistic, anti-androgenic, and anti-estrogenic potencies of 2-isopropylthioxanthone (ITX) as determined by in vitro bioassays and gene expression profiling
Peijnenburg.A, et al.
Toxicology in vitro, 24, 1619-1628 (2010)
Thi Kim Hoang Trinh et al.
Physical chemistry chemical physics : PCCP, 21(31), 17036-17046 (2019-07-30)
Although N-heterocyclic carbenes (NHCs) have brought profound changes in catalytic organic synthesis, their generation generally requires an inert atmosphere and harsh conditions. To overcome these limitations, an air-stable NHC photogenerator has been developed involving two mild components: 1,3-bis(mesityl)imidazolium tetraphenylborate (IMesH+BPh4-)
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