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Dihydralazine sulfate Sale

(Synonyms: 硫酸双肼屈嗪, Dihydralazine sulphate, Depressan, Hydralazine sulfate, 1,4-Dihydrazinophthalazine sulfate, Nepresol) 目录号 : GC20103

Dihydralazine sulfate 是一种抗高血压的药物。

Dihydralazine sulfate Chemical Structure

Cas No.:7327-87-9

规格 价格 库存 购买数量
10 mg
¥265.00
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25 mg
¥478.00
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50 mg
¥683.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Dihydralazine sulphate is an antihypertensive agent. 

Chemical Properties

Cas No. 7327-87-9 SDF
别名 硫酸双肼屈嗪, Dihydralazine sulphate, Depressan, Hydralazine sulfate, 1,4-Dihydrazinophthalazine sulfate, Nepresol
分子式 C8H12N6O4S 分子量 288.28
溶解度 DMSO: 6 mg/mL(20.8 mM) 储存条件 Store at RT
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为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 3.4688 mL 17.3442 mL 34.6885 mL
5 mM 0.6938 mL 3.4688 mL 6.9377 mL
10 mM 0.3469 mL 1.7344 mL 3.4688 mL
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Research Update

Dihydralazine sulfate analysis using 2-methyl-o-nitropyridine-6-carboxaldehyde

J Pharm Sci 1977 Jan;66(1):116-8.PMID:833726DOI:10.1002/jps.2600660132.

A sensitive, selective colorimetric assay was developed for the quantitative analysis of Dihydralazine sulfate. The method is based on the interaction of buffered (pH 4) Dihydralazine sulfate with a methanolic solution of 2-methyl-3-nitropyridine-6-carboxaldehyde upon heating to give an orange color. This color can be quantified spectrophotometrically at 450 nm,with a lower limit of detection of 1 mug/ml. The color is stable for at least 24 hr. There is no interference from other drugs likely to be present along with Dihydralazine sulfate and common excipients. The method was used successfully for the determination of Dihydralazine sulfate in combination with other drugs in different commercial tablets. The developed method was applicable as a stability-indicating assay.

Flow-injection chemiluminescence determination of Dihydralazine sulfate in serum using luminol and diperiodatocuprate (III) system

Spectrochim Acta A Mol Biomol Spectrosc 2010 Jan;75(1):77-82.PMID:19910243DOI:10.1016/j.saa.2009.09.044.

A novel flow-injection chemiluminescence (CL) method for the determination of Dihydralazine sulfate (DHZS) is described. The method is based on the reaction of luminol and diperiodatocuprate (K(2)[Cu(H(2)IO(6))(OH)(2)], DPC) in alkaline medium to emit CL, which is greatly enhanced by DHZS. The possible CL mechanism was first proposed based on the kinetic characteristic, CL spectrum and UV spectra. The optimum condition for the CL reaction was in detail studied using flow-injection system. The experiments indicated that under optimum condition, the CL intensity was linearly related to the concentration of DHZS in the range of 7.0x10(-9) to 8.6x10(-7) g mL(-1) with a detection limit (3sigma) of 2.1x10(-9) g mL(-1). The proposed method had good reproducibility with the relative standard deviation 3.1% (n=7) for 5.2x10(-8) g mL(-1) of DHZS. This method has the advantages of simple operation, fast response and high sensitivity. The special advantage of the system is that very low concentration of luminol can react with DPC catalyzed by DHZS to get excellent experiment results. And CL cannot be observed nearly when luminol with same concentration reacts with other oxidants, so luminol-DPC system has higher selectivity than other luminol CL systems. The method has been successfully applied to determine DHZS in serum.

Chemiluminescence investigation of carbon dioxide-enhanced oxidation of Dihydralazine sulfate by peroxynitrite and its application to pharmaceutical analysis

Anal Chim Acta 2008 Jun 2;616(2):190-5.PMID:18482603DOI:10.1016/j.aca.2008.04.032.

A weak chemiluminescence (CL) emission was observed upon mixing peroxynitrite (ONOO(-)) with Dihydralazine sulfate (DHZS). Further experiments showed that carbonate media could enhance the CL emission significantly. Based on these observations, a novel flow injection CL method for the determination of DHZS is developed. The CL signal is linearly with DHZS concentration in the range of 0.01-3.0 microg mL(-1) with a detection limit of 3.6 ng mL(-1). The method was applied to the analysis of DHZS in pharmaceutical preparations and compared well with the high-performance liquid chromatography (HPLC) method. The CL mechanism is discussed and it is postulated that it involves nitrosoperoxocarboxylate (ONOOCO(2)(-)), which is an unstable adduct and can rapidly decompose into *NO(2) and *CO(3)(-) radical. The latter can then oxidize DHZS to give out strong CL emission.