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三乙胺

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Water; Glycerin; Sodium Laureth Sulfate; Polyethylene; Acrylates/C10-30 Alkyl Acrylate Crosspolymer; Lauryl Glucoside; Phenoxyethanol; Microcrystalline Wax; Fragrance; Methylparaben; Menthyl Lactate; Sodium Hydroxide; Tetrasodium EDTA; Cellulose; Lactose; Sodium Ascorbyl Phosphate; Acrylates/Ammonium Methacrylate Copolymer; Hydroxypropyl Methylcellulose; Mica; Talc; Titanium Dioxide; Tocopheryl Acetate; Triethyl Citrate; Cucumis Sativus Fruit Extract; Citrus Grandis Fruit Extract; Panax Ginseng Root Extract; Zingiber Officinale Root Extract; Iron Oxides; Red 30; Yellow 5; Yellow 5 Lake

水;甘油;钠Laureth硫酸盐;聚乙烯; Acrylates/C10-30烷基丙烯酸酯Crosspolymer ;十二烷基糖苷; Phenoxyethanol ;微晶蜡;香水; Methylparaben ;薄荷乳酸;氢氧化钠; Tetrasodium乙二胺四乙酸;纤维素;乳糖;钠抗坏血酸磷酸酯;丙烯酸酯/铵甲基丙烯酸共聚物;羟丙基甲基纤维素;云母;滑石粉;二氧化钛; Tocopheryl醋酸;三柠檬酸;黄瓜水果提取物;柚皮果提取物;人参根提取物;生姜根提取物;铁氧化物;红30 ;黄河5 ;黄河5湖

Water; Glycerin; Sodium Laureth Sulfate; Polyethylene; Acrylates/C10-30 Alkyl Acrylate Crosspolymer; Lauryl Glucoside; Phenoxyethanol; Microcrystalline Wax; Fragrance; Methylparaben; Menthyl Lactate; Sodium Hydroxide; Tetrasodium EDTA; Cellulose; Lactose; Sodium Ascorbyl Phosphate; Acrylates/Ammonium Methacrylate Copolymer; Hydroxypropyl Methylcellulose; Mica; Talc; Titanium Dioxide; Tocopheryl Acetate; Triethyl Citrate; Cucumis Sativus Fruit Extract; Citrus Grandis Fruit Extract; Panax Ginseng Root Extract; Zingiber Officinale Root Extract; Iron Oxides; Red 30; Yellow 5; Yellow 5 Lake.

成分Ingredients 水;甘油;钠Laureth硫酸盐;聚乙烯; Acrylates/C10-30烷基丙烯酸酯Crosspolymer ;十二烷基糖苷; Phenoxyethanol ;微晶蜡;香水; Methylparaben ;薄荷乳酸;氢氧化钠; Tetrasodium乙二胺四乙酸;纤维素;乳糖;钠抗坏血酸磷酸酯;丙烯酸酯/铵甲基丙烯酸共聚物;羟丙基甲基纤维素;云母;滑石粉;二氧化钛; Tocopheryl醋酸;三柠檬酸;黄瓜水果提取物;柚皮果提取物;人参根提取物;生姜根提取物;铁氧化物;红30 ;黄河5 ;黄河5湖

Furthermore, influences of different phosphate salts at various concentrations on the ionization efficiency of phosphopeptide were investigated systematically, finding that the signal intensity for phosphopeptide 48FQEEQQQTEDELQDK63 digested from β-casein were 5 to 8 times increased in an optimized condition with 10 mmol/L ammonium monobasic phosphate or 3 to 4 times increased with 10 mmol/L ammonium dibasic phosphate as additive to matrix 2,5-dihydroxybenzoic acid, respectively.

考察了两种适合于磷酸化肽离子化的基质类型2,5-二羟基苯甲酸和2,4,6-三羟基苯乙酮。用2,5-二羟基苯甲酸作为基质时,当加入10 mM 磷酸氢二铵时,磷酸化蛋白质β-casein的磷酸肽 48FQEEQQQTEDELQDK63的离子化效率可以增强5-8倍,当加入10 mM磷酸二氢胺时,磷酸肽的离子化效率可以增强3-4倍。

With the in-situ single-stage self-metallization protocol,surface-silvered polyimide film has been prepared using pyromellitic dianhydride/ 4,4\'-oxydianiline-based polyimide as the matrix and (1,1,1-trifluoro-2,4-pentadionato)silveras the silver precursor.

在原位一步自金属化法中,以均苯四甲酸酐/4,4\'-二胺基二苯醚基聚酰亚胺为基体,以三氟乙酰丙酮银作为银的母体制备出了表面金属化的聚酰亚胺银复合薄膜。

Mercaptopropyl methyldimethoxysilane was synthesized by thiourea in the presence of tetramethylammonium iodine as a catalyst and mixed liquid containing ethylenediamine and trichloroethylene as a neutralizer, without solvent, in which the reaction temperature, catalysts ,neutralizer and their amounts were optimized.

以四甲基碘化铵为催化剂,乙二胺和三氯乙烯的复合液为中和剂,在无溶剂体系中,用硫脲法合成了甲基巯丙基二甲氧基硅烷。

Two oligosaccharides, a hexasaccharide fragment of group E Streptococcus polysaccharide and a tetrasaccharide repeating unit of E. coli O7: K98: H6, consisting of α-(1→2)-and α-(1→3)-linked rhamnose backbones were synthesized in a regio-and-stereoselective manner.

以三氯乙酰亚胺酯为供体,不保护或部分保护的糖为受体,成功地合成了以α-(1→2)-和-α(1→3)-交替连接的鼠李糖为主链的GroupE Streptococcus六糖和E.coli O7:K98:H6四糖。

Methods 42 cases of intractable heart failure were dividedinto 3 groups, and received intravenous infusion of nesiritide (12 cases), glycerol trinitrate (15 cases), and dobutamine (15 cases) respectively. Plasma rennin activity, aldosterone and angiotensin II were measured before and after infusion in 24h and 48h.

42例患者分成三组:甲组应用rhBNP;乙组应用硝酸甘油;丙组应用多巴酚丁胺静脉注射,同时检测血浆肾素活性、血管紧张素II、血浆醛固酮浓度,并在24、48h再次复查上述指标,复查左室射血分数,进行比较。

N-dodecylethylenediaminetriacetic acid is a new type of chelating surfactants, which were in need of developing non-phorus detergents.

N-十二烷基乙二胺三乙酸是一种新型螯合性表面活性剂,是应无磷洗涤剂的研发要求而问世的。

Our method featured employing the glycosyl donor with Bz as the protectivegroups and 0.05 equiv of TMSOTf as the promoter.

即:用苯甲酰基保护的三氯乙酰亚胺酯作给体,用5%当量的TMSOTf作促进剂,在室温下反应5min至15min。

Our method featured employing the glycosyl donor with Bz as the protective groups and 0.05 equiv of TMSOTF as the promoter.

即:用苯甲酰基保护的三氯乙酰亚胺酯作给体,用 5%当量的 TMSOTf 作促进剂,在室温下反应 5 min 至 15 min。

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