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1,4-哌嗪二乙胺

更新时间:2025-08-22 10:17:31

1,4-哌嗪二乙胺结构式
1,4-哌嗪二乙胺结构式
品牌特惠专场
常用名 1,4-哌嗪二乙胺 英文名 Piperazine-1,4-diethylamine
CAS号 6531-38-0 分子量 172.271
密度 1.0±0.1 g/cm3 沸点 302.2±10.0 °C at 760 mmHg
分子式 C8H20N4 熔点 N/A
MSDS N/A 闪点 151.4±7.0 °C

 1,4-哌嗪二乙胺名称

中文名 N,N'-二(氨乙基)-哌嗪
英文名 2-[4-(2-aminoethyl)piperazin-1-yl]ethanamine
中文别名 N,N'-二(2-氨乙基)-哌嗪,1,4-哌嗪二乙胺 | 1,4-哌嗪二乙胺 | N,N'-二(2氨乙基)-哌嗪
英文别名 更多

 1,4-哌嗪二乙胺物理化学性质

密度 1.0±0.1 g/cm3
沸点 302.2±10.0 °C at 760 mmHg
分子式 C8H20N4
分子量 172.271
闪点 151.4±7.0 °C
精确质量 172.168793
PSA 58.52000
LogP -1.97
InChIKey PAOXFRSJRCGJLV-UHFFFAOYSA-N
SMILES NCCN1CCN(CCN)CC1
蒸汽压 0.0±0.6 mmHg at 25°C
折射率 1.512

 1,4-哌嗪二乙胺安全信息

危险品运输编码 UN 1760
包装等级 II
海关编码 2933599090

 1,4-哌嗪二乙胺合成线路

~87%

1,4-哌嗪二乙胺结构式

1,4-哌嗪二乙胺

6531-38-0

文献:Filosa, Rosanna; Peduto, Antonella; Micco, Simone Di; Caprariis, Paolo de; Festa, Michela; Petrella, Antonello; Capranico, Giovanni; Bifulco, Giuseppe Bioorganic and Medicinal Chemistry, 2009 , vol. 17, # 1 p. 13 - 24

~%

1,4-哌嗪二乙胺结构式

1,4-哌嗪二乙胺

6531-38-0

文献:European Journal of Organic Chemistry, , # 6 p. 1050 - 1055

~81%

1,4-哌嗪二乙胺结构式

1,4-哌嗪二乙胺

6531-38-0

文献:J. Gen. Chem. USSR (Engl. Transl.), , vol. 58, # 9 p. 2098 - 2102,1868 - 1871

~%

1,4-哌嗪二乙胺结构式

1,4-哌嗪二乙胺

6531-38-0

文献:Journal of Organic Chemistry USSR (English Translation), , vol. 23, p. 330 - 332 Zhurnal Organicheskoi Khimii, , vol. 23, # 2 p. 370 - 372

~75%

1,4-哌嗪二乙胺结构式

1,4-哌嗪二乙胺

6531-38-0

文献:Ganin, E.V.; Makarov, V.F.; Nikitin, V.I. Journal of Organic Chemistry USSR (English Translation), 1987 , vol. 23, p. 330 - 332 Zhurnal Organicheskoi Khimii, 1987 , vol. 23, # 2 p. 370 - 372

~%

1,4-哌嗪二乙胺结构式

1,4-哌嗪二乙胺

6531-38-0

文献:Journal of Organic Chemistry USSR (English Translation), , vol. 23, p. 330 - 332 Zhurnal Organicheskoi Khimii, , vol. 23, # 2 p. 370 - 372

 1,4-哌嗪二乙胺海关

海关编码 2933599090
中文概述 2933599090. 其他结构上有嘧啶环的化合物(包括其他结构上有哌嗪环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 1,4-哌嗪二乙胺靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
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 1,4-哌嗪二乙胺英文别名

2-[4-(2-Amino-ethyl)-piperazin-1-yl]-ethylamine
2,2'-(1,4-Piperazinediyl)diethanamine
1,4-Piperazinediethanamine
Piperazine-1,4-diethylamine
2,2'-piperazine-1,4-diyldiethanamine
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