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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Preparative separation and identification of novel subsidiary colors of the color additive D&C Red No. 33 (Acid Red 33) using spiral high-speed counter-current chromatography
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Preparative separation and identification of novel subsidiary colors of the color additive D&C Red No. 33 (Acid Red 33) using spiral high-speed counter-current chromatography

机译:螺旋高速逆流色谱法分离和鉴定色料D&C Red No.33(Acid Red 33)的新辅助色

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摘要

Three low-level subsidiary color impurities (A, B, and C) often present in batches of the color additive D&C Red No. 33 (R33, Acid Red 33, Colour Index No. 17200) were separated from a portion of R33 by spiral high-speed counter-current chromatography (HSCCC). The separation involved use of a very polar solvent system, 1-BuOH/5 mM aq. (NH4)(2)SO4. Addition of ammonium sulfate to the lower phase forced partition of the components into the upper phase, thereby eliminating the need to add a hydrophobic counterion as was previously required for separations of components from sulfonated dyes. The very polar solvent system used would not have been retained in a conventional multi-layer coil HSCCC instrument, but the spiral configuration enabled retention of the stationary phase, and thus, the separation was possible. A 1 g portion of R33 enriched in A, B, and C was separated using the upper phase of the solvent system as the mobile phase. The retention of the stationary phase was 38.1%, and the separation resulted in 4.8 mg of A of >90% purity, 18.3 mg of B of >85% purity, and 91 mg of C of 65-72% purity. A second separation of a portion of the C mixture resulted in 7 mg of C of >94% purity. The separated impurities were identified by high-resolution mass spectrometry and NMR spectroscopic techniques as follows: 5-amino-3-bipheny1-3-ylazo-4-hydroxy-naphthalene2,7-disulfonic acid, A; 5-amino-4-hydroxy-6-pheny1-3-phenylazo-naphthalene-2,7-disulfonic acid, B; and 5-amino-4-hydroxy-3,6-bis-phenylazo-naphthalene-2,7-disulfonic acid, C. The isomers A and B are compounds reported for the first time. Application of the spiral HSCCC method resulted in the additional benefit of yielding 930 mg of the main component of R33, 5-amino-4-hydroxy-3-phenylazo-naphthalene2,7-disulfonic acid, of >97% purity. Published by Elsevier B.V.
机译:通过螺旋分离法将R33的一部分中经常存在的三种低级辅助色杂质(A,B和C)批量添加为D&C红色33号(R33,酸性红33,颜色索引号17200)高速逆流色谱(HSCCC)。分离涉及使用极性极强的溶剂系统1-BuOH / 5 mM aq。 (NH4)(2)SO4。将硫酸铵添加到下层相中迫使组分分配到上层相中,从而消除了如先前从磺化染料中分离出组分所需要的那样添加疏水抗衡离子的需要。使用的极性极强的溶剂系统将无法保留在常规的多层线圈HSCCC仪器中,但是螺旋结构能够保留固定相,因此可以进行分离。使用溶剂系统的上层相作为流动相,分离出1 g富含A,B和C的R33。固定相的保留率为38.1%,分离得到4.8 mg的A> 90%纯度,18.3 mg的B> 85%纯度和91 mg的C 65-72%纯度。再次分离一部分C混合物,得到7 mg纯度> 94%的C。分离的杂质通过高分辨率质谱和NMR光谱技术鉴定如下:5-氨基-3-联苯基1-3-偶氮-4-羟基-萘2,7-二磺酸A; 5-氨基-4-羟基-6-苯基1-3-苯基偶氮-萘-2,7-二磺酸,B;异构体A和B是首次报道的化合物。和5-氨基-4-羟基-3,6-双-苯基偶氮-萘-2,7-二磺酸C。螺旋HSCCC方法的应用带来了额外的好处,即产生930 mg纯度> 97%的R33主要成分5-氨基-4-羟基-3-苯基偶氮-萘2,7-二磺酸。由Elsevier B.V.发布

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