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Piperazine - Wikipedia
https://en.m.wikipedia.org/wiki/Piperazine
Chemistry. Piperazine is freely soluble in water and ethylene glycol, but insoluble in diethyl ether. It is a weak base with two pK b of 5.35 and 9.73 at 25 °C.; the pH of a 10% aqueous solution of piperazine is 10.8–11.8. Piperazine readily absorbs water and carbon dioxide from the air.
DA: 18 PA: 22 MOZ Rank: 8
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Piperazine anhydrous for synthesis 110-85-0 - MilliporeSigma
https://www.sigmaaldrich.com/US/en/product/mm/807325
Piperazine anhydrous. Write a review. Ask a question. for synthesis. Synonym (s): Piperazine anhydrous, Diethylenediamine. Empirical Formula (Hill Notation): C4H10N2. CAS Number: 110-85-0. Molecular Weight: 86.14. MDL number: MFCD00005953. EC Index Number: 203-808-3. 8073250005. $34.00. Availability.
DA: 39 PA: 23 MOZ Rank: 69
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Piperazine anhydrous CAS 110-85-0 | 807325 - Merck
https://www.merckmillipore.com/IN/en/product/Piperazine-anhydrous,MDA_CHEM-807325
Piperazine anhydrous for synthesis. CAS 110-85-0, pH 12 (150 g/l, H₂O, 20 °C). Piperazine anhydrous MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents. SDS. CoA. Required Licenses. Synonyms: Diethylenediamine. CAS #: 110-85-0 EC Number: 203-808-3 Molar Mass: 86.14 g/mol Hill Formula: C₄H₁₀N₂.
DA: 41 PA: 87 MOZ Rank: 19
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Piperazine | C4H10N2 | CID 4837 - PubChem
https://pubchem.ncbi.nlm.nih.gov/compound/piperazine
Mol wt 194.23. Crystals from water (containing 44.34% anhydrous piperazine), mp 44 °C. bp 125-130 °C. Freely soluble in water; soluble in alcohol (about 1:2). Practically insoluble in ether. pH of a 10% aqueous solution 5.0-6.0 /Hexahydrate/
DA: 84 PA: 46 MOZ Rank: 59
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Piperazine anhydrous - Piperazine anhydrous - MilliporeSigma
https://www.sigmaaldrich.com/US/en/substance/piperazineanhydrous8614110850
Product Number. Description. Pricing. 8.07325. Piperazine anhydrous, for synthesis. Expand. Choose up to 4 products to compare. Compare. Piperazine anhydrous. Synonyms: Piperazine anhydrous. CAS 110-85-0. Molecular Weight 86.14. Browse Piperazine anhydrous and related products at Merck.
DA: 44 PA: 65 MOZ Rank: 37
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Piperazine - NIST Chemistry WebBook
https://webbook.nist.gov/cgi/cbook.cgi?ID=110-85-0
IUPAC Standard InChIKey: GLUUGHFHXGJENI-UHFFFAOYSA-N Copy CAS Registry Number: 110-85-0 Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Other names: Hexahydropyrazine; Antiren; Diethylenediamine; Diethyleneimine; Dispermine; Eraverm; Lumbrical; Piperazidine; Pipersol; Pyrazine hexahydride ...
DA: 28 PA: 91 MOZ Rank: 68
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Piperazine Anhydrous | Sigma-Aldrich - MilliporeSigma
https://www.sigmaaldrich.com/US/en/product/sigma/p3896
Piperazine Anhydrous; EC Number: 203-808-3; find Sigma-Aldrich-P3896 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldrich
DA: 41 PA: 42 MOZ Rank: 46
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Piperazine - NIST Chemistry WebBook
https://webbook.nist.gov/cgi/cbook.cgi?ID=C110850&Mask=1E9F
Steele, W.V.; Chirico, R.D.; Knipmeyer, S.E.; Nguyen, A.; Smith, N.K., Thermocynamic Properties and Ideal-Gas Enthalpies of Formation for Carbonate, Piperazine, Hexachloroprop-1-ene, Tetrakis(dimethylamino) ethylene, N,N'-Bis(2-hydroxyethyl)ethylenediamine, and 1,2,4-Tr, J. Chem. Eng. Data, 1997, 42, 1037-52.
DA: 92 PA: 99 MOZ Rank: 85
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Piperazine, anhydrous, 99%, Thermo Scientific Chemicals - Fisher Sci
https://www.fishersci.com/shop/products/piperazine-anhydrous-99-thermo-scientific/AAA1504922
Description. Piperazine acts as an intermediate for pharmaceuticals, polymers, dyes, corrosion inhibitors, rubber accelerators and surfactants. It is used as a raw material in the manufacture of plastics, polyamide resins, urethane and brake fluid. It is also used for carbondioxide and hydrogen sulfide gas scrubbing mediums.
DA: 9 PA: 41 MOZ Rank: 27
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Piperazine: Uses, Interactions, Mechanism of Action | DrugBank …
https://go.drugbank.com/drugs/DB00592
Jun 13, 2005 · Piperazine is an organic compound that consists of a six-membered ring containing two opposing nitrogen atoms. First used as a solvent for uric acid, the use of piperazine as an anthelmintic agent was first introduced in 1953. Upon entry into the systemic circulation, the drug is partly oxidized and partly eliminated as an unchanged compound.
DA: 34 PA: 92 MOZ Rank: 14