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文件

COA/COQ

8.08607

Trichloroisocyanuric acid

Name: Trichloroisocyanuric acid
Brand: MM

for synthesis

同義詞:

Trichloroisocyanuric acid, 1,3,5-Trichlorohexahydro-1,3,5-triazine-2,4,6-trione, 1,3,5-Trichloro-1,3,5-triazine-2,4,6-trione, TCCA, Bleaching solution

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About This Item

經驗公式（希爾表示法）:

C₃Cl₃N₃O₃

CAS號碼:

87-90-1

分子量：:

232.41

MDL號碼:

MFCD00006553

分類程式碼代碼:

12352115

酶委員會索引編號:

201-782-8

NACRES:

NA.22

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品質等級

200

形狀

crystals

效力

406 mg/kg LD₅₀, oral (Rat)
>2000 mg/kg LD₅₀, skin (Rabbit)

pH值

2.0-2.7 (20 °C, 10 g/L in H₂O)

mp

225-230 °C (decomposition)

轉變溫度

flash point >250 °C

密度

2.07 g/cm³

體積密度

850 kg/m³

儲存溫度

2-30°C

InChI

1S/C3Cl3N3O3/c4-7-1(10)8(5)3(12)9(6)2(7)11

InChI 密鑰

YRIZYWQGELRKNT-UHFFFAOYSA-N

應用

Catalyst- and metal-free C(sp2)–H bond selenylation of (N-hetero)-arenes using diselenides and trichloroisocyanuric acid at room temperature: An eco-friendly approach for the C(sp2)–H bond selenylation of imidazopyridines and other N-heteroarenes as well as simple arenes at ambient temperatures (JSS Neto et al., 2023).

Organic impurity profiling of 3, 4-methylenedioxyamphetamine (MDA) synthesised from helional: This paper explores the use of trichloroisocyanuric acid in the oxidative rearrangement reaction for synthesizing MDA, presenting an alternative oxidizing agent approach (AL Mercieca et al., 2023).

Convenient synthesis of 2-chloro-3-substituted quinoxalines by visible-light-induced radical cascade cyclization of ortho-diisocyanoarenes with sulfinic acids: This research discusses the use of trichloroisocyanuric acid as a Cl-source in visible-light-induced reactions, enhancing the synthesis process (P Natarajan et al., 2024).

Synergy between UV light and trichloroisocyanuric acid on methylisothiazolinone degradation: The study presents an advanced oxidation process using ultraviolet and trichloroisocyanuric acid for the degradation of MIT, detailing performance, kinetics, and pathways (Z Chai et al., 2023).