1,2,3,4-四氢萘

47篇引用文献

COA

级别和纯度:

无水级

≥99%

CAS编号: 119-64-2
分子式: C₁₀H₁₂
分子量: 132.2
Beilstein号: 1446407
MDL号: MFCD00001733
PubChem编号: 8404
PubChem SID: 504751666

有货

库存信息

关闭

库存信息

关闭

库存信息

关闭

货号 (SKU)	包装规格	是否现货
T119673-100ml	100ml	现货
T119673-500ml	500ml	现货
T119673-1L	1L	现货

查看相关系列

光谱试剂 (247)

Skip to the end of the images gallery

Skip to the beginning of the images gallery

基本描述

别名	萘满
英文别名	THN \| Bacticin \| Tetrahydronaphthalene \| InChI=1/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H \| 1,2,3,4-tetrahydronapthalene \| Benzocyclohexane \| F1908-0164 \| AI3-01257 \| AKOS000121383 \| T0713 \| TETRALIN [HSDB] \| Tetralin solvent \| WLN: L66 & TJ \|
规格或纯度	无水级, ≥99%
英文名称	1,2,3,4-Tetrahydronaphthalene
应用	检验锰。脱脂剂。中间体。萘、油类和树脂的溶剂
储存温度	避光
运输条件	常规运输
产品介绍	随储存时间而变暗。有似苯和甲醇的混合气味。能随水蒸气挥发。能与乙醇、丁醇、乙醚、丙酮、苯、氯仿、萘烷和石油醚混溶，溶于甲醇(50.6%w/w),不溶于水。露置空气中能产生四氢萘过氧化物，蒸馏时能与四氢萘作用发生爆炸，可加对苯二酚抗氧剂。低毒，半数致死量(大鼠，经口)2.86g/kg。有刺激性。检验锰。脱脂剂。中间体。萘、油类和树脂的溶剂
纯度	≥99%

关联靶点（人）

TSHR Tclin Thyroid stimulating hormone receptor (29986 活性数据)

点击查看靶蛋白信息： TSHR

活性类型	Relation	Activity value	Units	Action Type	期刊	PubMed Id	doi	Assay Aladdin ID

作用机制

作用机制	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	参考文献

名称和识别符

PubChem SID	504751666
分子类型	小分子
IIUPAC Name	1,2,3,4-tetrahydronaphthalene
INCHI	1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2
InChi Key	CXWXQJXEFPUFDZ-UHFFFAOYSA-N
Smiles	C1CCC2=CC=CC=C2C1
Isomeric SMILES	C1CCC2=CC=CC=C2C1
PubChem CID	8404
UN Number	1993
Packing Group	I
分子量	132.2
Beilstein号	1446407

化学和物理性质

溶解性	不溶于水；水中溶解度：47 mg/l 28 °C；可混溶于氯仿、乙醇、丙酮、苯、乙醚；可溶于甲醇、苯胺
密度	0.973
折光率	1.54135
闪点(℃)	(closed cup)77℃
沸点	207.2°C
熔点	-31.0°C
分子量	132.200 g/mol
XLogP3	3.500
氢键供体数Hydrogen Bond Donor Count	0
氢键受体数Hydrogen Bond Acceptor Count	0
可旋转键计数Rotatable Bond Count	0
精确质量Exact Mass	132.094 Da
单同位素质量Monoisotopic Mass	132.094 Da
拓扑极表面积Topological Polar Surface Area	0.000 Å²
重原子数Heavy Atom Count	10
形式电荷Formal Charge	0
复杂度Complexity	92.600
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	1

安全和危险性（GHS）

象形图	GHS07, GHS09
信号词	危险
危险声明	H227: 可燃液体 H302: 吞食有害 H305: 吞咽并进入呼吸道可能致命 H314: 造成严重的皮肤灼伤和眼睛损伤 H336: 可能引起嗜睡或头晕 H371: 可能会损坏器官 H401: 对水生生物有毒 H411: 对水生生物有毒并具有长期持续影响
预防措施声明	P264: 处理后要彻底洗手。 P273: 避免释放到环境中。 P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。 P321: 特殊处理（请参阅此标签上的...）。 P391: 收集溢出物 P302+P352: 如皮肤沾染：用水充分清洗。 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。 P362+P364: 脱掉沾污的衣服，清洗后方可重新使用。 P501: 将内容物/容器处理到。。。 P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。 P337+P317: 如果眼睛刺激持续：寻求医疗帮助。 P332+P317: 如果出现皮肤刺激：请寻求医疗帮助。
WGK Germany	2
Class	3
Merck Index	9221

质检证书（CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):

输入批号以搜索分析图谱:

通过匹配包装上的批号来查找并下载产品的 COA，每批产品都进行了严格的验证，您可放心使用！

找到13个结果

批号(Lot Number)	证书类型	货号
J2023020	分析证书	T119673
F2417355	分析证书	T119673
F2417392	分析证书	T119673
A2423269	分析证书	T119673
A2423275	分析证书	T119673
A2423277	分析证书	T119673
A2423268	分析证书	T119673
A2423276	分析证书	T119673
J1908100	分析证书	T119673
B2208423	分析证书	T119673
B2208424	分析证书	T119673
B2208425	分析证书	T119673
K2317059	分析证书	T119673

显示更多⌵

此产品的引用文献

如何在您的发表作品中引用阿拉丁的产品和网站? 引用文献检索

引用文献

1. Brodney MA, Auperin DD, Becker SL, Bronk BS, Brown TM, Coffman KJ, Finley JE, Hicks CD, Karmilowicz MJ, Lanz TA et al.. (2011) Design, synthesis, and in vivo characterization of a novel series of tetralin amino imidazoles as γ-secretase inhibitors: discovery of PF-3084014.. Bioorg Med Chem Lett, 21 (9): (2637-40). [PMID:21269827]
2. J Sikkema,J A de Bont. (1993-02-01) Metabolism of tetralin (1,2,3,4-tetrahydronaphthalene) in Corynebacterium sp. strain C125.. Applied and environmental microbiology, 59 ((2)): (567-572). [PMID:8434923]
3. Satish Chandra Puri,Asiya Nazir,Raman Chawla,Rajesh Arora,S Riyaz-Ul-Hasan,Touseef Amna,Bilal Ahmed,Vijeshwar Verma,Shikha Singh,Ravinder Sagar,Ashok Sharma,Raj Kumar,Rakesh Kumar Sharma,Ghulam Nabi Qazi. (2005-12-27) The endophytic fungus Trametes hirsuta as a novel alternative source of podophyllotoxin and related aryl tetralin lignans.. Journal of biotechnology, 122 ((4)): (494-510). [PMID:16375985]
4. Desire D Tshala-Katumbay,Valerie S Palmer,Michael R Lasarev,Robert J Kayton,Mohammad I Sabri,Peter S Spencer. (2006-07-29) Monocyclic and dicyclic hydrocarbons: structural requirements for proximal giant axonopathy.. Acta neuropathologica, 112 ((3)): (317-324). [PMID:16874529]
5. George Chiu,Charles Gluchowski,Carlos Forray. (2006-08-03) Design and synthesis of an alpha1a-adrenergic receptor subtype-selective antagonist from BE2254.. Chemical biology & drug design, 67 ((6)): (437-439). [PMID:16882319]
6. Hans-Jürgen Federsel,Martin Hedberg,Fredrik R Qvarnström,Magnus P T Sjögren,Wei Tian. (2007-08-03) Construction of a chiral central nervous system (CNS)-active aminotetralin drug compound based on a synthesis strategy using multitasking properties of (S)-1-phenylethylamine.. Accounts of chemical research, 40 ((12)): (1377-1384). [PMID:17668920]
7. Jun Kim,Kalidas Biswas,Ki-Won Jhon,Soon-Yong Jeong,Wha-Seung Ahn. (2009-05-16) Synthesis of AlPO4-5 and CrAPO-5 using aluminum dross.. Journal of hazardous materials, 169 ((1-3)): (919-925). [PMID:19442445]
8. Takahiro Matsumoto,Kei Ohkubo,Kaoru Honda,Akiko Yazawa,Hideki Furutachi,Shuhei Fujinami,Shunichi Fukuzumi,Masatatsu Suzuki. (2009-06-18) Aliphatic C-H bond activation initiated by a (mu-eta2:eta2-peroxo)dicopper(II) complex in comparison with cumylperoxyl radical.. Journal of the American Chemical Society, 131 ((26)): (9258-9267). [PMID:19530656]
9. Aroa López-Sánchez,Elena Rivas-Marín,Olga Martínez-Pérez,Belén Floriano,Eduardo Santero. (2009-08-18) Co-ordinated regulation of two divergent promoters through higher-order complex formation by the LysR-type regulator ThnR.. Molecular microbiology, 73 ((6)): (1086-1100). [PMID:19682246]
10. Bin Ma,Kevin M Guckian,Edward Yin-Shiang Lin,Wen-Cherng Lee,Daniel Scott,Gnanasambandam Kumaravel,Timothy L Macdonald,Kevin R Lynch,Cheryl Black,Sowmya Chollate,Kyungmin Hahm,Gregg Hetu,Ping Jin,Yi Luo,Ellen Rohde,Anthony Rossomando,Robert Scannevin,Joy Wang,Chunhua Yang. (2010-03-02) Stereochemistry-activity relationship of orally active tetralin S1P agonist prodrugs.. Bioorganic & medicinal chemistry letters, 20 ((7)): (2264-2269). [PMID:20188554]
11. Edlene O Santos,Luciano S Lima,Jorge M David,Lidiane C Martins,Maria Lenise S Guedes,Juceni P David. (2010-03-18) Podophyllotoxin and other aryltetralin lignans from Eriope latifolia and Eriope blanchetii.. Natural product research, 25 ((15)): (1450-1453). [PMID:20234970]
12. Qingyian Liu,Wenyuan Qian,Aiwen Li,Kaustav Biswas,Jian Jeffrey Chen,Christopher Fotsch,Nianhe Han,Chester Yuan,Leyla Arik,Gloria Biddlecome,Eileen Johnson,Gondi Kumar,Dianna Lester-Zeiner,Gordon Y Ng,Randall W Hungate,Benny C Askew. (2010-06-25) Aryl sulfonamides containing tetralin allylic amines as potent and selective bradykinin B1 receptor antagonists.. Bioorganic & medicinal chemistry letters, 20 ((15)): (4593-4597). [PMID:20573508]
13. Laura Ledesma García,Elena Rivas-Marín,Belén Floriano,Rita Bernhardt,Kerstin Maria Ewen,Francisca Reyes-Ramírez,Eduardo Santero. (2010-11-12) ThnY is a ferredoxin reductase-like iron-sulfur flavoprotein that has evolved to function as a regulator of tetralin biodegradation gene expression.. The Journal of biological chemistry, 286 ((3)): (1709-1718). [PMID:21068394]
14. M Pilar Ruiz,Jimmy Faria,Min Shen,Santiago Drexler,Teerawit Prasomsri,Daniel E Resasco. (2011-07-14) Nanostructured carbon-metal oxide hybrids as amphiphilic emulsion catalysts.. ChemSusChem, 4 ((7)): (964-974). [PMID:21751419]
15. Fabrizio Croccolo,Marc-Alexandre Arnaud,Didier Bégué,Henri Bataller. (2011-07-27) Concentration dependent refractive index of a binary mixture at high pressure.. The Journal of chemical physics, 135 ((3)): (034901-034901). [PMID:21787022]
16. Laura Tomás-Gallardo,Eduardo Santero,Belén Floriano. (2012-05-29) Involvement of a putative cyclic amp receptor protein (CRP)-like binding sequence and a CRP-like protein in glucose-mediated catabolite repression of thn genes in Rhodococcus sp. strain TFB.. Applied and environmental microbiology, 78 ((15)): (5460-5462). [PMID:22636000]
17. Mark W Grafton,Louis J Farrugia,Hans Martin Senn,Andrew Sutherland. (2012-07-06) Discovery of a multi-bond forming, four-step tandem process: construction of drug-like polycyclic scaffolds.. Chemical communications (Cambridge, England), 48 ((64)): (7994-7996). [PMID:22763364]
18. Zere Konuspayeva,Pavel Afanasiev,Thanh-Son Nguyen,Luca Di Felice,Franck Morfin,Nhat-Tai Nguyen,Jaysen Nelayah,Christian Ricolleau,Z Y Li,Jun Yuan,Gilles Berhault,Laurent Piccolo. (2015-03-15) Au-Rh and Au-Pd nanocatalysts supported on rutile titania nanorods: structure and chemical stability.. Physical chemistry chemical physics : PCCP, 17 ((42)): (28112-28120). [PMID:25765742]
19. F Aladar Bencsath,Ronald A Benner,Ann Abraham,Yuesong Wang,Kathleen R El Said,Edward L E Jester,Steven M Plakas. (2015-03-23) Screening for petrochemical contamination in seafood by headspace solid-phase microextraction gas chromatography-mass spectrometry.. Analytical and bioanalytical chemistry, 407 ((14)): (4079-4090). [PMID:25796529]
20. Tiago Souza Dos Santos,Jéssica Krüger,Fernando Falkenburger Melleu,Christina Herold,Karl Zilles,Anicleto Poli,Onur Güntürkün,José Marino-Neto. (2015-04-07) Distribution of serotonin 5-HT1A-binding sites in the brainstem and the hypothalamus, and their roles in 5-HT-induced sleep and ingestive behaviors in rock pigeons (Columba livia).. Behavioural brain research, 295 (45-63). [PMID:25843559]
21. Meredith C Schuman,Silke Allmann,Ian T Baldwin. (2015-04-16) Plant defense phenotypes determine the consequences of volatile emission for individuals and neighbors.. eLife, 4 [PMID:25873033]
22. H Bonilla-Jaime,G Guadarrama-Cruz,F J Alarcon-Aguilar,O Limón-Morales,G Vazquez-Palacios. (2015-06-13) Antidepressant-like activity of Tagetes lucida Cav. is mediated by 5-HT(1A) and 5-HT(2A) receptors.. Journal of natural medicines, 69 ((4)): (463-470). [PMID:26062718]
23. Guangming Jiang,Huiyuan Zhu,Xu Zhang,Bo Shen,Liheng Wu,Sen Zhang,Gang Lu,Zhongbiao Wu,Shouheng Sun. (2015-10-06) Core/Shell Face-Centered Tetragonal FePd/Pd Nanoparticles as an Efficient Non-Pt Catalyst for the Oxygen Reduction Reaction.. ACS nano, 9 ((11)): (11014-11022). [PMID:26434498]
24. Jia Liu,Jiechen Wang,Zhitao Zhang,Francisco Molina-Lopez,Ging-Ji Nathan Wang,Bob C Schroeder,Xuzhou Yan,Yitian Zeng,Oliver Zhao,Helen Tran,Ting Lei,Yang Lu,Yi-Xuan Wang,Jeffrey B-H Tok,Reinhold Dauskardt,Jong Won Chung,Youngjun Yun,Zhenan Bao. (2020-07-06) Fully stretchable active-matrix organic light-emitting electrochemical cell array.. Nature communications, 11 ((1)): (3362-3362). [PMID:32620794]
25. Jordi Casanovas,Adriana M Namba,R da Silva,Carlos Alemán. (2005-11-18) DFT-GIAO study of aryltetralin lignan lactones: conformational analyses and chemical shifts calculations.. Bioorganic chemistry, 33 ((6)): (484-492). [PMID:16289684]
26. Olga Martínez-Pérez,Aroa López-Sánchez,Francisca Reyes-Ramírez,Belén Floriano,Eduardo Santero. (2007-03-14) Integrated response to inducers by communication between a catabolic pathway and its regulatory system.. Journal of bacteriology, 189 ((10)): (3768-3775). [PMID:17351041]
27. Aroa López-Sánchez,Belén Floriano,Eloisa Andújar,Maria José Hernáez,Eduardo Santero. (2009-11-10) Tetralin-induced and ThnR-regulated aldehyde dehydrogenase and beta-oxidation genes in Sphingomonas macrogolitabida strain TFA.. Applied and environmental microbiology, 76 ((1)): (110-118). [PMID:19897762]
28. Laura Tomás-Gallardo,Eduardo Santero,Emilio Camafeita,Enrique Calvo,Michael Schlömann,Belén Floriano. (2009-03-01) Molecular and biochemical characterization of the tetralin degradation pathway in Rhodococcus sp. strain TFB.. Microbial biotechnology, 2 ((2)): (262-273). [PMID:21261920]
29. (2011-06-21) Toxicology and carcinogenesis studies of tetralin (CAS No. 119-64-2) in F344/N rats and B6C3F1 mice (inhalation studies).. National Toxicology Program technical report series, (561) ((561)): (1-198). [PMID:21685956]
30. Amrit Jalan,Richard H West,William H Green. (2013-01-11) An extensible framework for capturing solvent effects in computer generated kinetic models.. The journal of physical chemistry. B, 117 ((10)): (2955-2970). [PMID:23301874]
31. Qifeng Yang, Yiming Mo. (2023) Direct Electrochemical Oxidation of Benzylic C–H Bond by La2O3@C/CP Composite Electrode with Water as the Green Oxygen Source. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 62 (46): (19427–19436). [10.1021/acs.iecr.3c02229]
32. Jiaxing Chen, Shufang Wu, Xinlin Zhang, Yongjun Liu. (2023) Few-Layered Defect-Rich MoS2 Nanosheets with Ni Doping as Catalysts for Efficient Hydrodesulfurization Reaction. ACS Applied Nano Materials, 6 (20): (18812–18822). [10.1021/acsanm.3c02953]
33. Hao Shi, Zengqiang Mao, Longchao Ran, Candong Ru, Shengwei Guo, Hua Dong. (2023) Heavy oil viscosity reduction through aquathermolysis catalyzed by Ni20(NiO)80 nanocatalyst. FUEL PROCESSING TECHNOLOGY, 250 (107911). [10.1016/j.fuproc.2023.107911]
34. Wang Zhongze, Shi Haonan, Shu Sihao, Zhang Xing, Feng Shangzhen, Chen Jixiang. (2023) Metal–organic framework-derived carbon coated Ni–In intermetallic compounds for in-situ selective hydrogenation of methyl palmitate to hexadecanol in aqueous phase using methanol as hydrogen donor. Reaction Kinetics Mechanisms and Catalysis, 136 (4): (2021-2037). [10.1007/s11144-023-02435-7]
35. Lin Ai, Haonan Shi, Jixiang Chen. (2023) In-situ deoxygenation of methyl palmitate to hydrocarbons on highly dispersed Ni–Re/TiO2 catalyst in aqueous phase using methanol as a hydrogen donor. JOURNAL OF THE ENERGY INSTITUTE, 109 (101265). [10.1016/j.joei.2023.101265]
36. Hefei Wang, Zeming Wang, Jibao Deng, Jian Wang, Yanzheng Gao. (2023) Conductive black carbon promoted biotransformation of undissolved 2, 2′-dinitrobiphenyl by mediating electron transfer. SCIENCE OF THE TOTAL ENVIRONMENT, 882 (163619). [PMID:37080299] [10.1016/j.scitotenv.2023.163619]
37. Sihao Shu, Zhongze Wang, Xing Zhang, Haonan Shi, Shangzhen Feng, Jixiang Chen. (2023) Efficient deoxygenation of methyl esters to hydrocarbons on Al2O3 supported Ni-Sn intermetallic compounds. Molecular Catalysis, 540 (113056). [10.1016/j.mcat.2023.113056]
38. Jiaojiao Fang, Chengyang Zhu, Yaru Ni, Chunhua Lu, Zhongzi Xu. (2023) Double local electromagnetic fields collaboratively enhanced triplet–triplet annihilation upconversion for efficient photocatalysis. Catalysis Science & Technology, 13 (7): (2151-2159). [10.1039/D2CY01649D]
39. Hongye Cheng, Guojin Zhang, Yaxi Zhang, Zhen Song, Zhiwen Qi. (2023) Solute structure effect on aromatics-alkanes extractive separation toward rational LCO upgrading. SEPARATION AND PURIFICATION TECHNOLOGY, 310 (123213). [10.1016/j.seppur.2023.123213]
40. Chen Chen, Qiong Tang, Hong Xu, Mingxing Tang, Xuekuan Li, Lei Liu, Jinxiang Dong. (2023) Alkyl-tetralin base oils synthesized from coal-based chemicals and evaluation of their lubricating properties. CHINESE JOURNAL OF CHEMICAL ENGINEERING, 58 (20). [10.1016/j.cjche.2022.12.011]
41. Jiayao Qi, Yanni Guo, Hanqiong Jia, Binbin Fan, Hang Gao, Bo Qin, Jinghong Ma, Yanze Du, Ruifeng Li. (2023) Unpredictable properties of industrial HY zeolite for tetralin hydrocracking. FUEL PROCESSING TECHNOLOGY, 240 (107586). [10.1016/j.fuproc.2022.107586]
42. Wang Li, Wen-Ying Li, Xing-Bao Wang, Jie Feng. (2022) Radical-induced pyrolysis mechanism in Cal–O and Cal–Cal bond cleavage. FUEL PROCESSING TECHNOLOGY, 238 (107494). [10.1016/j.fuproc.2022.107494]
43. Gu Xiaoyu, Shi Haonan, Wang Dandan, Chen Jixiang. (2022) Glucose-derived carbon-coated Ni–In intermetallic compounds for in situ aqueous phase selective hydrogenation of methyl palmitate to hexadecanol. Reaction Kinetics Mechanisms and Catalysis, 135 (3): (1621-1634). [10.1007/s11144-022-02221-x]
44. Zhen Ge, Hongye Cheng, Guojin Zhang, Linsheng Wang, Zhiwen Qi. (2022) Mechanism of Extractive Separation of Light Cycle Oil Using a Deep Eutectic Solvent Composed of Tetrabutylphosphonium Bromide and Levulinic Acid. ENERGY & FUELS, 36 (4): (1854–1862). [10.1021/acs.energyfuels.1c03856]
45. Zeng Xingye, Adesina Adeyemo, Li Ping, Wang Hanlu, Zhou Rujin. (2022) Enhanced adsorptive-oxidative desulfurization of dibenzothiophene over Ti-MWW using cumene hydroperoxide as oxidant. KOREAN JOURNAL OF CHEMICAL ENGINEERING, 39 (1): (96-108). [10.1007/s11814-021-0844-y]
46. Zhi-Cong Wang, Dabo Chen, Ya-Qi Shan, Lin-Xin Lin, Pei-Gao Duan. (2022) Catalytic hydrotreatment of the high-boiling-point fraction of soybean straw biocrude in a mixed hydrogen donor. FUEL, 310 (122126). [10.1016/j.fuel.2021.122126]
47. Lei Chen, Zhi-Cong Wang, Dabo Chen, Lin-Xin Yin, Pei-Gao Duan. (2021) Hydro-upgrading of algal bio-oil in tetralin for the production of high-quality liquid fuel: Process intensification. FUEL PROCESSING TECHNOLOGY, 224 (107034). [10.1016/j.fuproc.2021.107034]
48. Bo Yan, Guangpeng Zhang, Peng Gao, He Li, Shuhang Ren, Weize Wu. (2021) Dissolution behavior of hydrogen in the model recycle solvent of mild direct coal liquefaction. FUEL PROCESSING TECHNOLOGY, 223 (106982). [10.1016/j.fuproc.2021.106982]
49. Zhuang Zeng, Zhuoshi Li, Shaoxia Guo, Jing Lv, Shouying Huang, Yue Wang, Xinbin Ma. (2021) Janus Au–Fe2.2C Catalyst for Direct Conversion of Syngas to Higher Alcohols. ACS Sustainable Chemistry & Engineering, 9 (33): (11258–11268). [10.1021/acssuschemeng.1c04263]
50. Lihua Zhu, Huaze Zhu, Mohsen Shakouri, Linghai Zeng, Zhiqing Yang, Yongfeng Hu, Hengqiang Ye, Hui Wang, Bing Hui Chen, Rafael Luque. (2021) Mechanistic insights into interfacial nano-synergistic effects in trimetallic Rh-on-NiCo on-CNTs for room temperature solvent-free hydrogenations. APPLIED CATALYSIS B-ENVIRONMENTAL, 297 (120404). [10.1016/j.apcatb.2021.120404]
51. Shisheng Liang, Yucui Hou, Weize Wu, He Li, Zhuosen He, Shuhang Ren. (2021) Residues characteristics and structural evolution of Naomaohu coal during a mild direct liquefaction process. FUEL PROCESSING TECHNOLOGY, 215 (106753). [10.1016/j.fuproc.2021.106753]
52. Tinghao Jia, Lun Pan, Xiaoyu Wang, Jiawei Xie, Si Gong, Yunming Fang, Hua Liu, Xiangwen Zhang, Ji-Jun Zou. (2021) Mechanistic insights into the thermal oxidative deposition of C10 hydrocarbon fuels. FUEL, 285 (119136). [10.1016/j.fuel.2020.119136]
53. Zhiming Wu, Qian Zeng, Hongye Cheng, Lifang Chen, Zhiwen Qi. (2020) Extractive separation of tetralin-dodecane mixture using tetrabutylphosphonium bromide-based deep eutectic solvent. Chemical Engineering and Processing-Process Intensification, 149 (107822). [10.1016/j.cep.2020.107822]
54. Jiaojiao Fang, Cihui Zhou, Yukai Chen, Liang Fang, Wei Wang, Cheng Zhu, Yaru Ni, Chunhua Lu. (2020) Efficient Photocatalysis of Composite Films Based on Plasmon-Enhanced Triplet–Triplet Annihilation. ACS Applied Materials & Interfaces, 12 (1): (717–726). [PMID:31813218] [10.1021/acsami.9b17954]
55. Jiaojiao Fang, Yukai Chen, Wei Wang, Liang Fang, Chunhua Lu, Cheng Zhu, Jiahui Kou, Yaru Ni, Zhongzi Xu. (2019) Highly efficient photocatalytic hydrogen generation of g-C3N4-CdS sheets based on plasmon-enhanced triplet–triplet annihilation upconversion. APPLIED CATALYSIS B-ENVIRONMENTAL, 258 (117762). [10.1016/j.apcatb.2019.117762]
56. Zhi-Cong Wang, Pei-Gao Duan, Xiao-Jie Liu, Feng Wang, Yu-Ping Xu. (2019) Hydrotreating the Low-Boiling-Point Fraction of Biocrude in Hydrogen Donor Solvents for Production of Trace-Sulfur Liquid Fuel. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 58 (24): (10210–10223). [10.1021/acs.iecr.9b01274]
57. Shilei Ding, Zhixia Li, Fuwei Li, Zhaohe Wang, Jiangfeng Li, Tingting Zhao, Hongfei Lin, Congjin Chen. (2018) Catalytic hydrogenation of stearic acid over reduced NiMo catalysts: Structure–activity relationship and effect of the hydrogen-donor. APPLIED CATALYSIS A-GENERAL, 566 (146). [10.1016/j.apcata.2018.08.028]
58. Shanshan Jie, Congqiang Yang, Yuan Chen, Zhigang Liu. (2018) Facile synthesis of ultra-stable Co-N-C catalysts using cobalt porphyrin and peptides as precursors for selective oxidation of ethylbenzene. Molecular Catalysis, 458 (1). [10.1016/j.mcat.2018.08.007]
59. Xu Yu-Ping, Duan Pei-Gao, Wang Feng, Guan Qing-Qing. (2018) Liquid fuel generation from algal biomass via a two-step process: effect of feedstocks. Biotechnology for Biofuels, 11 (1): (1-16). [PMID:29619079] [10.1186/s13068-018-1083-2]
60. Ming Li, Dong Liu, Bin Lou, Yadong Zhang, Shitao Yu, Jnuwei Ding. (2018) Hydroalkylation modification of naphthene-based aromatic-rich fraction and its influences on mesophase development. RSC Advances, 8 (7): (3750-3759). [PMID:35542897] [10.1039/C7RA12619K]
61. Lihua Zhu, Huan Zhang, Laifu Zhong, Jinbao Zheng, Changlin Yu, Nuowei Zhang, Bing Hui Chen. (2018) RuNiCo-based nanocatalysts with different nanostructures for naphthalene selective hydrogenation. FUEL, 216 (208). [10.1016/j.fuel.2017.12.023]
62. Yuan Chen, Shanshan Jie, Congqiang Yang, Zhigang Liu. (2017) Active and efficient Co-N/C catalysts derived from cobalt porphyrin for selective oxidation of alkylaromatics. APPLIED SURFACE SCIENCE, 419 (98). [10.1016/j.apsusc.2017.04.246]
63. Tang Jia, Zhou Bin, Zhang Shilin, Wang Zhuang, Xiong Lei, Li Peng. (2015) Synthesis and photocatalytic properties of lotus-rootlike Au-ZnO nanostructures. Science China-Chemistry, 58 (5): (858-862). [10.1007/s11426-014-5307-4]
64. Xianjie Gong, Yongsheng Guo, Juan Xiao, Yuzhong Yang, Wenjun Fang. (2012) Densities, Viscosities, and Refractive Indices of Binary Mixtures of 1,2,3,4-Tetrahydronaphthalene with Some n-Alkanes at T = (293.15 to 313.15) K. JOURNAL OF CHEMICAL AND ENGINEERING DATA, 57 (11): (3278–3282). [10.1021/je300899n]
65. Xizhuang Qin, Tao Shen, Guanbo Li, Lei Shi, Zhenyu Liu, Qingya Liu. (2024) A coal constituent based kinetic model for direct coal liquefaction. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 94 (310). [10.1016/j.ijhydene.2024.11.017]
66. Niu Menglong, Pan Liuyi, Ji Panpan, Liu Ning, Ge Yiqing, Niu Ben, Ma Baoqi. (2024) A preliminary study on the co-hydrogenation process of coal tar and bio-oil. Reaction Kinetics Mechanisms and Catalysis, 137 (3): (1667-1682). [10.1007/s11144-024-02614-0]
67. Qingqing Li, Zhiwei Sun, Yilin Wei, Zixu Ma, Liucheng Wang, Renfeng Nie. (2024) Acceptorless ambient-temperature dehydrogenation and reversible hydrogenation of N-heterocycles over single-atom Co-N-C catalysts. APPLIED CATALYSIS B-ENVIRONMENTAL, 351 (123959). [10.1016/j.apcatb.2024.123959]
68. Haonan Shi, Sihao Shu, Zhongze Wang, Xing Zhang, Xiaoyu Gu, Jixiang Chen. (2024) Efficient and robust ultrathin porous carbon encapsulated Ni–Sn intermetallic compounds derived from metal–organic frameworks for in-situ aqueous phase deoxygenation of fatty acid methyl esters. JOURNAL OF THE ENERGY INSTITUTE, 114 (101587). [10.1016/j.joei.2024.101587]
69. Min Han, Lexuan Zhao, Hongye Cheng, Zhiwen Qi. (2024) Enhancing fractionation of terpenoids and terpenes in citrus essential oils by a biphasic extraction system. CHEMICAL ENGINEERING SCIENCE, 299 (120476). [10.1016/j.ces.2024.120476]
70. Weikang Gao, Chuanlei Liu, Yuxiang Chen, Guanchu Guo, Hao Wang, Fengjing Yang, Hao Jiang, Qiyue Zhao, Qiumin Wu, Benxian Shen, Hui Sun. (2024) Exploring ionic liquids for the extraction separation of aromatic hydrocarbons from diesel via multiple interaction analyses coupled with experimental evaluation. FUEL, 368 (131634). [10.1016/j.fuel.2024.131634]
71. Runtian Xia, Naixin Wang, Xinheng Cai, Jing Yang, Hongyu Liu, Zelong Liu, Haomiao Liu, Qundan Zhang, Zhiping Tao, Wei Wang. (2025) Impact of dopant solvents on the characterization of complex organic mixtures by atmospheric pressure photoionization source. FUEL, 381 (133628). [10.1016/j.fuel.2024.133628]
72. Shangzhen Feng, Hantao Zhou, Zhongze Wang, Sihao Shu, Xing Zhang, Jixiang Chen. (2024) In-situ aqueous phase hydrodeoxygenation of methyl palmitate on Ni-Co alloy embedded in mesoporous carbon hollow spheres catalysts. NEW JOURNAL OF CHEMISTRY, [10.1039/D3NJ04975B]
73. Huanjin Jiang, Jie Yang, Shangzhen Feng, Hantao Zhou, Jixiang Chen. (2024) In-Situ Hydrodeoxygenation of Methyl Palmitate on a TiO2–ZrO2 Supported Ni3Sn2 Intermetallic Compound with Methanol as a Hydrogen Donor in the Aqueous Phase. ENERGY & FUELS, 38 (21): (21245-21254). [10.1021/acs.energyfuels.4c03638]
74. Yongming Zeng, Tianchi Xu, Weizhi Chen, Jianglin Fang, Dongzhong Chen. (2024) Quasi-chromophores Segregated by Single-chain Nanoparticles of Fluorinated Zwitterionic Random Copolymers Showing Remarkably Enhanced Fluorescence Emission Capable of Fluorescent Cell Imaging. MACROMOLECULAR RAPID COMMUNICATIONS, (2400029). [PMID:38477018] [10.1002/marc.202400029]
75. Jiang Huanjin, Yang Jie, Wang Wenhao, Fang Hailong, Chen Jixiang. (2025) Resorcinol–Formaldehyde Resin and Sodium Dodecyl Sulfate Co-assisted Mesoporous TiO2 Supported Ni3Sn2 Intermetallic Compound Catalysts for In-Situ Hydrodeoxygenation of Methyl Palmitate with Methanol as the Hydrogen Donor in Water. CATALYSIS SURVEYS FROM ASIA, (1-13). [10.1007/s10563-025-09451-8]
76. Mingshuo Chi, Jianpeng Cui, Jianwen Hu, Junjie Fan, Senchang Du, Peiwen Xiao, Songqing Hu, Shuangqing Sun. (2024) Silica Janus nanosheets anchored with Ni nanoparticles for in-situ upgrading and stimulus-responsive demulsification to enhance heavy oil recovery. JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 181 (106603). [10.1016/j.jaap.2024.106603]
77. Ke Zhao, Jianzhao Cao, Ying Qi, Peng Wei, Jian Cheng, Yahong Xie. (2024) Synthesis of multilayer graphene and its graphene derivatives from coal. PHYSICA SCRIPTA, 99 (3): (035924). [10.1088/1402-4896/ad2327]

溶液计算器

摩尔浓度计算器

计算溶液所需的质量、体积或浓度。

质量

浓度

体积

分子量

g/mol

稀释计算器

计算配制储备溶液所需的稀释度。

浓度1（C1）

体积 1 (V1)

浓度 2 (C2)

体积 2 (V2)

复溶计算器

复溶计算器允许您快速计算试剂的体积，以复溶小瓶。只需输入试剂的质量和目标浓度，计算器将确定其余部分。

体积（添加到小瓶中）

质量（小瓶）

所需的复溶浓度