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Supelco

2-Isopropylthioxanthone

PESTANAL®, analytical standard

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C16H14OS
Número CAS:
5495-84-1
Peso molecular:
254.35
Número CE:
226-827-9
Número MDL:
MFCD00055658
Código UNSPSC:
41116107
ID de substância PubChem:
329754906
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

linha de produto

PESTANAL®

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

environmental

Formato

neat

cadeia de caracteres 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

chave InChI

KTALPKYXQZGAEG-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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.

Produtos recomendados

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.

Informações legais

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

Pictogramas

Health hazardEnvironment
GHS08,GHS09

Palavra indicadora

Warning

Frases de perigo

H361f,H410

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

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

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCK2348
BCBX4608

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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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