CAS: 3055-94-5; Triethylene Glycol Monododecyl Ether
该化合物是非离子表面活性剂,具有水利和亲脂性,在各种应用中有用,来自三乙基甘醇和多德卡诺醇,形成一种结构,提高水和有机溶剂的溶解性.该化合物一般是无色的,可粉黄液,粘度相对较低.该化合物具有极好的乳化,湿润和散射特性,在个人护理产品,洗涤剂和工业应用的配方中具有价值.此外,三乙基乙醇单丁基醚以温度著著称,适合用于化妆剂.其低毒性和生物降解性进一步增强了其在有环境意识的配方中的吸引力.
- 英文名称Triethylene Glycol Monododecyl Ether
- 中文名称三甘醇单正十二烷基醚
- IUPAC名称2-(2-(2-(dodecyloxy)ethoxy)ethoxy)ethan-1-ol
- 其它别名Lauryl Triethoxylate; 2-(2-(2-(Dodecyloxy)Ethoxy)Ethoxy)Ethanol; Cl15H93Xtm; (2S)-2-Acetamido-3-Methyl-3-Sulfanylbutanoic Acid; Triethylene Glycol Mono-N-Dodecyl Ether; Triethyleneglycol Monolauryl Ether; 4,6-Dichloropyrimidin-2-Ylami
- CAS编号3055-94-5
- MFCD编号:MFCD00042659
- EINECS号:221-280-2
- FDA UNII编号:F32E4CB0UJ
- 分子式:C18H38O4
- 分子量:318.5
- 产品CID: 1291334
- 产品分类有机原料→分子砌块→脂肪链类化合物
相似化合物
3055-99-0 19327-39-0 5274-63-5物理性质
MSDS等安全信息
欧盟法规
ECHA物质ECHA物质C&L通报REACH预注册上下游产品
十二烷基二乙二醇醚 Diethylene Glycol Monododecyl Ether 3055-93-4乙二醇单十二烷基醚 3-Oxapentadecan-1-Ol 4536-30-5
合成工艺路线路线简述
- 合成目标产物 Triethylene Glycol Mono-N-Dodecyl Ether 主要起始原料 1-Iododecane And Triethylene Glycol
- (文献来源)合成步骤主要原料 1-Iododecane 和 Triethylene Glycol
乙二醇单十二烷基醚置于boron Trifluoride Diacetate体系中,化学反应生成3-十二烷醇
参考文献:Chakhovskoy Et Al.,Bulletin Des Societes Chimiques Belges,1956,Vol. 65,P. 453,470
标题:Chakhovskoy Et Al.,Bulletin Des Societes Chimiques Belges,1956,Vol. 65,P. 453,470
海关参考信息
- 2905121000-正丙醇
2905130000-正丁醇
2905310000-1,2-乙二醇
2909110000-乙醚 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:US-2012190064-A1
优先权日:2004-10-01
标题 :Feeding buffers, systems, and methods for in vitro synthesis of biomolecules
发明人：KUDLICKI WIESLAW ANTONI; KEPPETIPOLA SHIRANTHI; FLETCHER JULIA; GETBEHEAD ASHLEY ELAINE; KATZEN FEDERICO; VOZZA-BROWN LAURA
权利人:KUDLICKI WIESLAW ANTONI; KEPPETIPOLA SHIRANTHI; FLETCHER JULIA; GETBEHEAD ASHLEY ELAINE; KATZEN FEDERICO; VOZZA-BROWN LAURA; LIFE TECHNOLOGIES CORP
摘要:Compositions, methods and kits for in vitro systems for synthesis of biomolecules such as polypeptides, are provided herein. Cell extracts that provide enhanced yields of soluble proteins using in vitro protein synthesis methods are provided. The invention also includes methods for producing high yields of proteins by the addition of a feeding solution that includes amino acids and an energy source to an ongoing in vitro synthesis system. The invention also includes methods of using a high-yield in vitro synthesis system to produce large quantities of proteins with incorporated labeled amino acids for analysis by methods such as by NMR. The invention further includes vectors for enhanced production of proteins from nucleic acid templates using in vitro synthesis systems.
专利号:US-2009209032-A1
优先权日:2004-10-01
标 题 :Feeding buffers, systems, and methods for in vitro synthesis of biomolecules
专利号:EP-1848812-A2
优先权日:2004-10-01
标题:Feeding buffers, systems, and methods for in vitro synthesis of biomolecules
专利号:US-2006110788-A1
优先权日:2004-10-01
标题 :Feeding buffers, systems, and methods for in vitro synthesis of biomolecules
专利号:UA-128971-C2
优先权日:2020-01-29
标 题:METHOD FOR SYNTHESIS OF AN AMINO ACID SURFACE-ACTIVE SUBSTANCE
专利号:WO-2006039622-A2
优先权日:2004-10-01
标 题 :Feeding buffers, systems, and methods for in vitro synthesis of biomolecules
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主要参考文献
[参考文献]: Nalawansha Da, Et Al. Protacs: An Emerging Therapeutic Modality In Precision Medicine. Cell Chem Biol. 2020;27(8):998-985.[参考文献]: Peter J Mcnamara, Et Al. Surfactants, Aromatic And Isoprenoid Compounds, And Fatty Acid Biosynthesis Inhibitors Suppress Staphylococcus Aureus Production Of Toxic Shock Syndrome Toxin 1. Antimicrob Agents Chemother. 2009 May;53(5):1898-906.
合成参考文献
摘要:S13 | EUCOSMETICS | Combined Inventory of Ingredients Employed in Cosmetic Products (2000) and Revised Inventory (2006) | DOI:10.5281/zenodo.2624118
摘要:S7 | EAWAGSURF | Eawag Surfactants Suspect List | DOI:10.5281/zenodo.2621971
摘要:International Journal of Toxicology 31(Suppl. 2):169-244, 2012
参考文献:10.1007/bf00114627
摘要:van Ginkel CG. Complete degradation of xenobiotic surfactants by consortia of aerobic microorganisms. Biodegradation. 1996 Apr;7(2):151–64. doi: 10.1007/bf00114627.
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