- Homopiperazine
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- $100.00 / 100Grams
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2024-04-26
- CAS:505-66-8
- Min. Order: 100Grams
- Purity: 99.99%
- Supply Ability: 100Tons
- Homopiperazine
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- $10.00 / 1kg
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2024-04-23
- CAS:505-66-8
- Min. Order: 1kg
- Purity: 99.6%
- Supply Ability: 100000
- Homopiperazine
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- $9.90 / 1kilogram
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2024-04-22
- CAS:505-66-8
- Min. Order: 1kilogram
- Purity: 99%
- Supply Ability: 40tons
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| | Homopiperazine Chemical Properties |
| Melting point | 38-40 °C (lit.) | | Boiling point | 169 °C (lit.) | | density | 0.95 | | refractive index | 1.4378 (estimate) | | Fp | 148 °F | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | solubility | Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Slightly) | | form | Crystalline Mass | | pka | 11.02±0.20(Predicted) | | color | White to light yellow | | Water Solubility | Soluble in water. | | Sensitive | Air Sensitive & Hygroscopic | | BRN | 102711 | | CAS DataBase Reference | 505-66-8(CAS DataBase Reference) | | NIST Chemistry Reference | Homopiperazine(505-66-8) | | EPA Substance Registry System | 1H-1,4-Diazepine, hexahydro- (505-66-8) |
| Hazard Codes | C,Xi | | Risk Statements | 21-34 | | Safety Statements | 26-36/37/39-45-27 | | RIDADR | UN 3259 8/PG 2 | | WGK Germany | 1 | | RTECS | HM3850000 | | F | 3-10-23 | | Hazard Note | Irritant/Corrosive | | TSCA | Yes | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29339900 |
| | Homopiperazine Usage And Synthesis |
| Important pharmaceutical intermediates | Homopiperazine is a nitrogen-containing seven-membered ring hetero-atomic compound and is an important pharmaceutical intermediate. The majority of its derivatives has strong biological activity and medicinal value and can be used for synthesizing homopiperazine hydrochloride, cyclizine, carbamazepine, chlorcyclizine and other drugs. Western medicine often takes homopiperazine as raw material for the modified quinoline and isoquinoline derivatives, quinolone derivative, thiazolidine carboxylic acid amide derivatives and other drugs, and for the synthesis of pyridazine, nitroxyl-containing benzylamine derivatives, water-soluble azole and other drugs which has good efficacy for the treatment of cardiovascular disease, interstitial plasma cell pneumonia especially for AIDS patients with Pneumocystis pneumonia, asthma, central nervous system disorders including depression and anxiety disorders. For example, 1-(5-isoquinoline-sulfonyl) homopiperazine hydrochloride is effective in the treatment of symptoms such as chronic angina disease, vitiligo, depression, anxiety, cerebral vasospasm and cerebral vasospasm caused cerebral ischemia and other symptoms.
Homopiperazine and its high-piperazine derivatives have become important pharmaceutical intermediates and have exhibited great potential of being sedative, anti-psychotic, anti-inflammatory and anti-neurotic and is an important product of a connecting link between the proceeding and the following in the chemical industry and pharmaceutical industry and have been widely applied to the pharmaceuticals, pesticides, surfactants, energetic materials and other fields.
Currently the domestic heterocyclic compounds are mainly used for producing the quinolone antibacterial drugs. This drug, through inhibiting the bacterial DNA gyrase, blocks the DNA replication and produces the antimicrobial effects. According to the report of ARMIGER H et al, after using homopiperazine as substitute of piperazine for the synthesis of drugs like cyclizine, homo-chlorcyclizine and other drugs, animal experiments had demonstrated that the activity of antihistamine drugs had been significantly enhanced. Its main products include quinoline and isoquinoline derivatives, quinolone derivative, thiazolidine carboxylic acid amide derivatives and other drugs, as well as the synthesis of disubstituted pyridazine, the nitroxyl-containing benzyl amine derivatives and water-soluble azole drug.
The derivative of homopiperazine molecule with the hydrogen atom in the amino group being substituted by long-chain alkyl or alkoxy can be used as wetting agents, emulsifying agents, detergents, coloring agents; homopiperazine and its derivatives, because of containing staining keratin filament, can be used as oxidation coloring agents and have vibrant colors and high solidness properties. It plays an important role in the dyeing, especially in the dyeing of human hair.
Polymers containing homopiperazine monomer have many unique properties such as being able to improve the melting point and improve their solubility. Resin and synthetic fiber containing such a polymer have been applied to a variety of special fields.
The above information is edited by the chemicalbook of Dai Xiongfeng.
| | Preparation | Homopiperazine can be synthesized using amino compounds such as N-(2-cyanoethyl)-ethylenediamine, N-(β-hydroxy)-1,3-propanediamine, ethylenediamine as raw material so that homopiperazine has various kinds of synthetic routes according to different raw materials.
With the development of China's petrochemical industry, for the synthesis of the starting raw material of homopiperazine, alcohols and ethylene diamine, it not only has low price but also can get high-quality product as well as extremely abundant source. Currently, though there are homopiperazine domestic manufacturers, but the technology is lagged behind, the quality is not high and the production output is limited, all the above points are in urgent need for being transformed and improved. From this perspective, it is imperative for accelerating the process of development of fine chemical products of homopiperazine with a wide range of application. Therefore, the market prospect of the homopiperazine is very broad.
Using ethylenediamine as the raw material: the method uses the easily available ethylenediamine as the initial raw material, further goes through sulfonylation, cyclization, de-sulfonylation, 3-step reaction for synthesizing homopiperazine with the total yield being 78%. Within this synthetic method, during the first step of ethylenediamine sulfonylation, the addition of a phase transfer catalyst can significantly improve the product yield with the yield being 86%. During the second step of cyclization reaction, selection of NaH/ DMF reaction system can enable the completion of the cyclization reaction under milder reaction conditions. Finally, under HBr/HAc/PhOH reaction conditions, remove the sulfonyl group with a yield being 91% to give the final product homopiperazine. The results indicate that it is an excellent homopiperazine synthesis route of various kinds of advantages including easily available raw materials, simple operation and high yield with certain prospects for industrial application.
| | Uses | It can be used as organic and pharmaceutical synthesis intermediates, for example, being applied to the synthesis of fasudil hydrochloride.
Homopiperazine acts as a corrosion inhibitor for iron. It has also been used in the preparation of potent H3 receptor antagonists for use as treatments for neurodegenerative conditions such as Alzheimer disease.
| | Chemical Properties | white to light yellow crystalline mass | | Uses | pharmaceutical intermediate | | Uses | Homopiperazine is used to prepare 1,4-bis-(2-thiazolyl)-1,4-diazacycloheptane by reacting with 2-bromo-thiazole. It acts as an intermediate for repaglinide and fasudil hydrochloride. It is also used in the preparation of potent H3 receptor antagonists, which is used for the treatment of neurodegenerative conditions. Further, it is used in vesicant, cosmetic, emulsifier and energetic material. It acts as a corrosion inhibitor for iron. In pharmaceuticals, it is employed as antipyretic and reducing blood sugar, adiposity, calm, antipsychotic and anti-nervous. | | structure and hydrogen bonding |
The conformation of Homopiperazine is shown below, and the N–C–C–N torsion angle of 58.2(4)° confirms that the left-hand end of the molecule has an almost ideal chair-type conformation, which is only slightly distorted by the insertion of the extra atom at the right-hand end. The two nitrogen lone pairs are aligned in opposite directions, which facilitates the formation of a hydrogen-bonded network due to interaction with the NH of adjacent molecules.
Crystal data for C5H12N2, M = 100.16 g mol-1, colorless prism, crystal dimensions 0.10 × 0.10 × 0.10 mm3, tetragonal, space group I–42d (No. 122), a = b = 7.208(2), c = 23.094(7) Å, α = β = γ = 90.00°, V = 1199.9(6) Å3, Z = 8, Dcalc = 1.109 g cm-3, T = 93 K, R1 = 0.0637, Rw2 = 0.1633 for 536 reflections with I > 2σ(I), and 37 variables, Rint 0.0374, goodness of fit on F2 1.137. Data have been deposited at the Cambridge Crystallographic Data Centre as CCDC 2049324[1].
| | References | [1] R. Aitken, A. Slawin, Dheirya K. Sonecha. “Homopiperazine (Hexahydro-1,4-diazepine).” Molbank 2021 1 (2021): M1200.
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| | Homopiperazine Preparation Products And Raw materials |
| Raw materials | Hydrochloric acid-->Ethyl acetate-->Methanol-->Diethyl ether-->Sulfuric acid-->Tetrahydrofuran-->Dichloromethane-->Acetic acid-->Sodium-->N,N-Dimethylformamide-->Toluene-->Potassium carbonate-->Chloroform-->Sodium sulfate-->Potassium hydroxide-->Triethylamine-->Ammonium hydroxide-->Acetone-->Ammonia-->Sodium bicarbonate-->Sodium hydride-->Sodium borohydride-->Hydrogen bromide-->Hydrogen-->1-Butanol-->Nickel-->Phenol-->Tosyl chloride-->Ethylenediamine-->Phosphorus tribromide-->tert-Butyl methyl ether-->Sulfurous Acid-->2,3-DICHLORO-5,8-DIHYDROXY-1,4-NAPHTHOQUINONE-->1,3-Dibromopropane-->1,3-Diaminopropane-->Malonaldehyde bis(diethyl acetal)-->Benzyltriethylammonium bromide-->Tetraoctylammonium bromide-->N,N'-Bis(ethylene)-p-Toluenesulfonamide-->Oxamide | | Preparation Products | 1-Boc-hexahydro-1,4-diazepine-->1-BENZYL-1,4-DIAZEPANE-->1-(4-FLUOROBENZYL)-1,4-DIAZEPANE-->BENZYL 1-HOMOPIPERAZINECARBOXYLATE-->N-ACETYLHOMOPIPERAZINE-->1-Formylhomopiperazine-->ethyl 1,4-diazepane-1-carboxylate-->1-(2-PHENYLETHYL)HOMOPIPERAZINE |
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