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Hydroxyamine hydrochloride Sale

(Synonyms: 羟胺盐酸盐) 目录号 : GC60917

Hydroxylammonium chloride (Hydroxylamine hydrochloride) is the hydrochloric acid salt of hydroxylamine, which is a biological intermediate in the nitrification and in the anammox.

Hydroxyamine hydrochloride Chemical Structure

Cas No.:5470-11-1

规格 价格 库存 购买数量
500mg
¥450.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Hydroxylammonium chloride (Hydroxylamine hydrochloride) is the hydrochloric acid salt of hydroxylamine, which is a biological intermediate in the nitrification and in the anammox.

Chemical Properties

Cas No. 5470-11-1 SDF
别名 羟胺盐酸盐
Canonical SMILES NO.[H]Cl
分子式 ClH4NO 分子量 69.49
溶解度 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 14.3906 mL 71.9528 mL 143.9056 mL
5 mM 2.8781 mL 14.3906 mL 28.7811 mL
10 mM 1.4391 mL 7.1953 mL 14.3906 mL
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Research Update

Determination of carbonyl compounds in pool water with O-(2,3,4,5,6-pentafluorobenzyl)Hydroxyamine hydrochloride and gas chromatographic-tandem mass spectrometric analysis

J Chromatogr A 2004 Aug 13;1046(1-2):293-6.PMID:15387201DOI:10.1016/j.chroma.2004.06.084.

To avoid microbiological decay pool water is disinfected, a procedure which results into a lot of disinfection by-products, like carbonyl compounds, as well as a large number of others. The carbonyl compounds dissolved in pool water were derivatisized with O-(2,3,4,5,6-pentafluorobenzyl)Hydroxyamine hydrochloride (PFBHA) and extracted using n-hexane. Measuring with the help of GC-electron-capture detection is hardly possible because of interferents like halogenated organics. Another method to detect the PFBHA derivates is the use of tandem mass spectrometry. Calibration ranges and precision are applicable and sufficient to determine carbonyl compounds in pool water.

The effects of active chlorine on photooxidation of 2-methyl-2-butene

Sci Total Environ 2011 Jun 1;409(13):2652-61.PMID:21524786DOI:10.1016/j.scitotenv.2011.03.038.

Active chlorine comprising hypochlorite (OCl⁻), hypochlorous acid (HOCl) and chlorine (Cl₂) is the active constituent in bleach formulations for a variety of industrial and consumer applications. However, the strong oxidative reactivity of active chlorine can cause adverse effects on both human health and the environment. In this study, aerosolized Oxone® [2KHSO₅, KHSO₄, K₂SO₄] with saline solution has been utilized to produce active chlorine (HOCl and Cl₂). To investigate the impact of active chlorine on volatile organic compound (VOC) oxidation, 2-methyl-2-butene (MB) was photoirradiated in the presence of active chlorine using a 2-m³ Teflon film indoor chamber. The resulting carbonyl products produced from photooxidation of MB were derivatized with O-(2,3,4,5,6-pentafluorobenzyl) Hydroxyamine hydrochloride (PFBHA) and analyzed using gas chromatograph-ion trap mass spectrometer (GC/ITMS). The photooxidation of MB in the presence of active chlorine was simulated with an explicit kinetic model using a chemical solver (Morpho) which included both Master Chemical Mechanism (MCM) and Cl radical reactions. The reaction rate constants of a Cl radical with MB and its oxidized products were estimated using a Structure-Reactivity Relationship method. Under dark conditions no effect of active chlorine on MB oxidation was apparent, whereas under simulated daylight conditions (UV irradiation) rapid MB oxidation was observed due to photo-dissociation of active chlorine. The model simulation agrees with chamber data showing rapid production of oxygenated products that are characterized using GC/ITMS. Ozone formation was enhanced when MB was oxidized in the presence of irradiated active chlorine and NO(x).

Humic acid as an efficient and reusable catalyst for one pot three-component green synthesis of 5-substituted 1 H-tetrazoles in water

RSC Adv 2020 Jan 3;10(2):784-789.PMID:35494449DOI:10.1039/c9ra08523h.

Humic acid is a non toxic, inexpensive, easily available high-molecular weight polymer. A simple and facile one pot three-component synthesis of 5-substituted 1H-tetrazoles from aldehydes, Hydroxyamine hydrochloride and sodium azide using humic acid as an efficient catalyst in water is described. The method reported has several advantages such as high to excellent yields, easy work-up, mild reaction conditions, use of water as a green solvent, and a commercially available, nontoxic and reusable catalyst.