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| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| T121851-5ml |
5ml |
现货 ![]() |
| |
| T121851-25ml |
25ml |
现货 ![]() |
| |
| T121851-50ml |
50ml |
现货 ![]() |
|
| 别名 | 四正丁基氢氧化膦 |
|---|---|
| 英文别名 | TBPH | SCHEMBL108027 | EINECS 238-528-0 | DFQPZDGUFQJANM-UHFFFAOYSA-M | TBPH solution | Phosphonium, tetrabutyl-, hydroxide (1:1) | AKOS015950702 | DTXSID70884758 | T2571 | MFCD00068456 | tetrabutylphosphanium;hydroxide | FT-0769999 | Tetrabutylphosphoniu |
| 规格或纯度 | 40 wt.% in H2O |
| 英文名称 | Tetrabutylphosphonium hydroxide solution(TBPH) |
| 应用 | Tetrabutylphosphonium hydroxide (TBPH) can be used: · To convert poorly water-soluble acidic APIs into TBP ionic liquids (IL). · As a cation source in the synthesis of Good′s buffer ionic liquids (GB-ILs) via an acid?base neutralization reaction with Good′s buffer anions. · To synthesize tetrabutylphosphonium acetate, which along with Cu2O-nanoparticles forms an excellent catalyst system for protodecarboxylation reactions |
| 运输条件 | 常规运输 |
| 产品介绍 |
Tetrabutylphosphonium hydroxide (TBPH) can be used: • To convert poorly water-soluble acidic APIs into TBP ionic liquids (IL). • As a cation source in the synthesis of Good′s buffer ionic liquids (GB-ILs) via an acid−base neutralization reaction with Good′s buffer anions. • To synthesize tetrabutylphosphonium acetate, which along with Cu2O-nanoparticles forms an excellent catalyst system for protodecarboxylation reactions Tetrabutylphosphonium hydroxide (TBPH) can be used: • To convert poorly water-soluble acidic APIs into TBP ionic liquids (IL). • As a cation source in the synthesis of Good′s buffer ionic liquids (GB-ILs) via an acid−base neutralization reaction with Good′s buffer anions. • To synthesize tetrabutylphosphonium acetate, which along with Cu2O-nanoparticles forms an excellent catalyst system for protodecarboxylation reactions |
| EC号 | 238-528-0 |
|---|---|
| 分子类型 | 小分子 |
| IIUPAC Name | tetrabutylphosphanium;hydroxide |
| INCHI | 1S/C16H36P.H2O/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H2/q+1;/p-1 |
| InChi Key | DFQPZDGUFQJANM-UHFFFAOYSA-M |
| Smiles | CCCC[P+](CCCC)(CCCC)CCCC.[OH-] |
| Isomeric SMILES | CCCC[P+](CCCC)(CCCC)CCCC.[OH-] |
| PubChem CID | 84487 |
| 分子量 | 276.44 |
| Beilstein号 | 4826225 |
| Reaxy-Rn | 4826225 |
| 溶解性 | Miscible with water |
|---|---|
| 密度 | 0.99 |
| 折光率 | 1.412 |
| 分子量 | 276.440 g/mol |
| XLogP3 | |
| 氢键供体数Hydrogen Bond Donor Count | 1 |
| 氢键受体数Hydrogen Bond Acceptor Count | 1 |
| 可旋转键计数Rotatable Bond Count | 12 |
| 精确质量Exact Mass | 276.258 Da |
| 单同位素质量Monoisotopic Mass | 276.258 Da |
| 拓扑极表面积Topological Polar Surface Area | 1.000 Ų |
| 重原子数Heavy Atom Count | 18 |
| 形式电荷Formal Charge | 0 |
| 复杂度Complexity | 116.000 |
| 同位素原子数Isotope Atom Count | 0 |
| 定义的原子立体中心计数Defined Atom Stereocenter Count | 0 |
| 未定义的原子立体中心计数Undefined Atom Stereocenter Count | 0 |
| 定义的键立体中心计数Defined Bond Stereocenter Count | 0 |
| 未定义的键立体中心计数Undefined Bond Stereocenter Count | 0 |
| 所有立体化学键的总数The total count of all stereochemical bonds | 0 |
| 共价键合单元计数Covalently-Bonded Unit Count | 2 |
| 一般危化品 | 一般危化品 |
|---|---|
| 象形图 | GHS05 |
| 信号词 | 危险 |
| 危险声明 |
H314: 造成严重的皮肤灼伤和眼睛损伤 H318: 造成严重的眼睛损伤 |
| 预防措施声明 |
P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。 P310: 立即致电解毒中心或医生。 P305+P351+P338: 如进入眼睛:用水小心冲洗几分钟。如戴隐形眼镜并可方便地取出,取出隐形眼镜。继续冲洗。 P405: 密闭存放 |
| WGK Germany | 3 |
| 个人防护装备 | Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter |
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| 批号(Lot Number) | 证书类型 | 货号 |
|---|---|---|
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 | |
| 分析证书 | T121851 |
| 1. Cecilia Springer,Edward Dere,Susan J Hall,Elizabeth V McDonnell,Simon C Roberts,Craig M Butt,Heather M Stapleton,Deborah J Watkins,Michael D McClean,Thomas F Webster,Jennifer J Schlezinger,Kim Boekelheide. (2012-09-28) Rodent thyroid, liver, and fetal testis toxicity of the monoester metabolite of bis-(2-ethylhexyl) tetrabromophthalate (tbph), a novel brominated flame retardant present in indoor dust.. Environmental health perspectives, 120 ((12)): (1711-1719). [PMID:23014847] |
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| 20. Siqi Zhang,Danielle Ireland,Nisha S Sipes,Mamta Behl,Eva-Maria S Collins. (2019-04-04) Screening for neurotoxic potential of 15 flame retardants using freshwater planarians.. Neurotoxicology and teratology, 73 (54-66). [PMID:30943442] |
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| 23. Nina Strah,Giulia Romano,Clelia Introna,Raffaella Klima,Marta Marzullo,Laura Ciapponi,Aram Megighian,Monica Nizzardo,Fabian Feiguin. (2020-03-29) TDP-43 promotes the formation of neuromuscular synapses through the regulation of Disc-large expression in Drosophila skeletal muscles.. BMC biology, 18 ((1)): (34-34). [PMID:32216790] |
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| 25. Takashi Miyamoto,Ryo Koyama,Naruki Kurokawa,Atsushi Hotta,Saman Alavi,Ryo Ohmura. (2020-08-09) Thermophysical Property Measurements of Tetrabutylphosphonium Oxalate (TBPOx) Ionic Semiclathrate Hydrate as a Media for the Thermal Energy Storage System.. Frontiers in chemistry, 8 (547-547). [PMID:32766205] |
| 26. Ryan J H West,Joanne L Sharpe,André Voelzmann,Anna L Munro,Ines Hahn,Richard A Baines,Stuart Pickering-Brown. (2020-09-08) Co-expression of C9orf72 related dipeptide-repeats over 1000 repeat units reveals age- and combination-specific phenotypic profiles in Drosophila.. Acta neuropathologica communications, 8 ((1)): (158-158). [PMID:32894207] |
| 27. Matheus M Pereira,João D Calixto,Ana C A Sousa,Bruno J Pereira,Álvaro S Lima,João A P Coutinho,Mara G Freire. (2020-09-12) Towards the differential diagnosis of prostate cancer by the pre-treatment of human urine using ionic liquids.. Scientific reports, 10 ((1)): (14931-14931). [PMID:32913223] |
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| 33. Wenbin Jin,Yuqi Ke,Xianxian Liu,Qiwei Yang,Zongbi Bao,Baogen Su,Qilong Ren,Yiwen Yang,Huabin Xing. (2017-04-08) Enhanced self-assembly for the solubilization of cholesterol in molecular solvent/ionic liquid mixtures.. Physical chemistry chemical physics : PCCP, 19 ((17)): (10835-10842). [PMID:28387400] |
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| 37. Luca Lo Piccolo,Rosa Bonaccorso,Andrea Attardi,Lorenzo Li Greci,Giulia Romano,Martina Sollazzo,Giorgio Giurato,Antonia Maria Rita Ingrassia,Fabian Feiguin,Davide F V Corona,Maria Cristina Onorati. (2018-04-05) Loss of ISWI Function in Drosophila Nuclear Bodies Drives Cytoplasmic Redistribution of Drosophila TDP-43.. International journal of molecular sciences, 19 ((4)): [PMID:29617352] |
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| 43. Lei Yuan, Leihao Zhang, Guilin Li, Shaojuan Zeng, Qizhou Xue, Chongyang Jiang, Xiangping Zhang. (2023) Phenoxy-Nitrile Bifunctional Ionic Liquid for Efficient Electroreduction of CO2 to Oxalate. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 62 (41): (16931–16938). [10.1021/acs.iecr.3c02876] |
| 44. Heming Zhang, Chan Meng, Qian Su, Li Dong, Wen Liu, Xiaokang Wang, Yunong Li, Weiguo Cheng. (2023) Sterically regulated halogen-free bifunctional ionic liquids for catalytic conversion of CO2 into cyclic carbonates. ChemistrySelect, 8 (37): (e202301015). [10.1002/slct.202301015] |
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| 46. Haolin Li, Lin Ma, Ping Wen, Yunyan Han, Rui Dong, Mingjin Fan. (2022) Molecular structure insight into the tribological behavior of sulfonate ionic liquids as lubricants for titanium alloys. JOURNAL OF MOLECULAR LIQUIDS, 357 (119082). [10.1016/j.molliq.2022.119082] |
| 47. Qiao Yang, Jingcheng Hao. (2022) Synthesis of metal sulfides via ionic liquid-mediated assembly strategy and their photocatalytic degradation of dyes in water. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 633 (127848). [10.1016/j.colsurfa.2021.127848] |
| 48. Ran Ping, Penghui Zhao, Qianqian Zhang, Guangyu Zhang, Fusheng Liu, Mengshuai Liu. (2021) Catalytic Conversion of CO2 from Simulated Flue Gases with Aminophenol-Based Protic Ionic Liquids to Produce Quinazoline-2,4(1H,3H)-diones under Mild Conditions. ACS Sustainable Chemistry & Engineering, 9 (14): (5240–5249). [10.1021/acssuschemeng.1c01466] |
| 49. Fangchao Cheng, Panpan Zhao, Tulong Ouyang, Jianping Sun, Yiqiang Wu. (2021) Comprehensive utilization strategy of cellulose in a facile, controllable, high-yield preparation process of cellulose nanocrystals using aqueous tetrabutylphosphonium hydroxide. GREEN CHEMISTRY, 23 (4): (1805-1815). [10.1039/D0GC04370B] |
| 50. Qiang Yuan, Jifeng Pang, Wenguang Yu, Mingyuan Zheng. (2020) Vapor-Phase Furfural Decarbonylation over a High-Performance Catalyst of 1%Pt/SBA-15. Catalysts, 10 (11): (1304). [10.3390/catal10111304] |
| 51. Fusheng Liu, Ran Ping, Yongqiang Gu, Penghui Zhao, Bin Liu, Jun Gao, Mengshuai Liu. (2020) Efficient One Pot Capture and Conversion of CO2 into Quinazoline-2,4(1H,3H)-diones Using Triazolium-Based Ionic Liquids. ACS Sustainable Chemistry & Engineering, 8 (7): (2910–2918). [10.1021/acssuschemeng.9b07242] |
| 52. Hao Wu, Zhaizhu Deng, Bijian Zhou, Minghui Qi, Minghuang Hong, Guobin Ren. (2019) Improved transdermal permeability of ibuprofen by ionic liquid technology: Correlation between counterion structure and the physicochemical and biological properties. JOURNAL OF MOLECULAR LIQUIDS, 283 (399). [10.1016/j.molliq.2019.03.046] |
| 53. Zhenhao Wei, Kake Zhu, Lanyu Xing, Fan Yang, Yunsheng Li, Yarong Xu, Xuedong Zhu. (2017) Steam-assisted transformation of natural kaolin to hierarchical ZSM-11 using tetrabutylphosphonium hydroxide as structure-directing agent: synthesis, structural characterization and catalytic performance in the methanol-to-aromatics reaction. RSC Advances, 7 (39): (24015-24021). [10.1039/C7RA03141F] |
| 54. Yanjun Gong, Qiongzheng Hu, Yongxian Guo, Li Yu. (2017) Photocatalyzed Reduction of Chromium(VI) and Thermal-Driven Heterogeneous Separation. ACS Sustainable Chemistry & Engineering, 5 (6): (4511–4516). [10.1021/acssuschemeng.7b00554] |
| 55. Jie Wang, Jielin Huang, Hui Xu, Li Dong, Songsong Chen, Junping Zhang, Suojiang Zhang. (2024) Phosphorus-modulated surface active center reconstruction in cerium oxide for polyols conversion into carbonates. APPLIED CATALYSIS B-ENVIRONMENTAL, 357 (124284). [10.1016/j.apcatb.2024.124284] |