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**1H-Pyrazole hydrochloride (1:1)** is a salt formed by the reaction of pyrazole with hydrochloric acid (HCl), where the protonation occurs at the nitrogen atom (N1) of the pyrazole ring. It can serve as a precursor for pyrazole complexes or undergo further reactions, such as deprotonation or coordination with metal chlorides, to form pyrazolium salts or metal-pyrazole coordination compounds. 1H-pyrazole hydrochloride (1:1) is also relevant in solid-state chemistry, where it participates in mechanochemical transformations to generate pyrazolium tetrachlorometallates or pyrazole-metal complexes. Additionally, pyrazolium-based derivatives, including hydrochlorides, have potential applications in energy storage as phase-change materials. **Other names for 1H-pyrazole hydrochloride (1:1) include:** Pyrazolium chloride, [H2pz]Cl.

35877-22-6

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35877-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35877-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,7 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35877-22:
(7*3)+(6*5)+(5*8)+(4*7)+(3*7)+(2*2)+(1*2)=146
146 % 10 = 6
So 35877-22-6 is a valid CAS Registry Number.

35877-22-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-pyrazole,hydrochloride

1.2 Other means of identification

Product number -
Other names pyrazole hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35877-22-6 SDS

35877-22-6Upstream product

35877-22-6Relevant academic research and scientific papers

Complex compounds based on 1-isopropenylimidazoles and -pyrazole

Zyryanova,Baikalova,Tarasova,Afonin,Kukhareva,Maksimova,Trofimov

, p. 1283 - 1289 (2005)

With respect to Co2+, Ni2+, Zn2+,Cd 2+, Cu2+, Pd2+, and Sn4+ salts, 1-isopropenyl-substituted imidazole, 2-methylimidazole, and pyrazole behave as monodentate ligands with only one coordination center on the N1 and N2 atoms, respectively; 1-isopropenylpyrazole under complex-formation conditions is dealkylated to form pyrazole complexes. The reaction with HCl leaves the unsaturated substituent in 1-isopropenylimidazole intact and yields corresponding hydrochlorides by the N3 atom of the heterocycle. The least basic 1-isopropenylpyrazole takes up HCl also by the double bond of the alkenyl group.

Coordination chemistry in the solid state: Synthesis and interconversion of pyrazolium salts, pyrazole complexes, and pyrazolate MOFs

Adams, Christopher J.,Kurawa, Mukhtar A.,Orpen, A. Guy

, p. 6974 - 6984 (2010)

Solid pyrazole reacts with HCl gas to form pyrazolium chloride [H 2pz]Cl, which reacts in the solid state, under grinding, with metal chlorides MCl2 (M = Co, Zn, Cu) to form the pyrazolium tetrachlorometallate salts [H2pz]2[MCl4] (M = Co 1, Zn 3, Cu 5). Salt 5 cannot be made in solution, and upon standing at room temperature spontaneously emits HCl to give the coordination compound [CuCl 2(Hpz)2] (6). Compounds 1 and 3 do not exhibit this behaviour, but can be ground together with bases such as KOH or K 2CO3 to effect the elimination of HCl and afford their respective [MCl2(Hpz)2] compounds (M = Co 2, Zn 4). 2, 4 and 6 can also be synthesised in the solid-state by direct reaction of the appropriate metal chloride with pyrazole, or by reaction of a basic metal salt such as the carbonate or hydroxide with pyrazolium chloride. 4 and 6 {and their nickel analogue [NiCl2(Hpz)2]} can be ground with a further two equivalents of base to make the known polymeric metal pyrazolates [M(pz)2]n (M = Ni 7, Cu 8, Zn 9); the same reaction appears to work for the cobalt analogue 2, but the presumed product [Co(pz) 2]n10 then decomposes by oxidation. The imidazolate complexes [M(im)2] (M = Ni, 11; Cu, 12; Zn, 13; Co, 14) were similarly prepared by grinding the appropriate [M(Him)2Cl 2] precursor with KOH. The Royal Society of Chemistry 2010.

Pyrazolium Phase-Change Materials for Solar-Thermal Energy Storage

Matuszek, Karolina,Vijayaraghavan,Forsyth, Craig M.,Mahadevan, Surianarayanan,Kar, Mega,MacFarlane, Douglas R.

, p. 159 - 164 (2020)

Thermal energy storage technology utilizing phase-change materials (PCMs) can be a promising solution for the intermittency of renewable energy sources. This work describes a novel family of PCMs based on the pyrazolium cation, that operate in the 100–200

Anti-inflammator 1,n-diarylpyrazol-3-amines

-

, (2008/06/13)

There are described compounds of formula I, STR1 in which either R2 represents hydrogen, alkyl or Ar2, and R3 represents hydrogen, alkyl or alkyl substituted by Ar3 ; or R2 and R3 together

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