
CAS 1356020-01-3
:Fórmula:C15H21N3O4S
InChI:InChI=1S/C15H21N3O4S/c1-15(2)12(14(21)22)18-10(23-15)7-17-13(20)11(16)8-3-5-9(19)6-4-8/h3-6,10-12,18-19H,7,16H2,1-2H3,(H,17,20)(H,21,22)/t10?,11-,12+/m1/s1
Chave InChI:HLJHSXSJKLJNKE-SAIIYOCFSA-N
SMILES:CC1([C@@H](NC(S1)CNC(=O)[C@@H](C2=CC=C(C=C2)O)N)C(=O)O)C
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(4S)-2-(((R)-2-Amino-2-(4-hydroxyphenyl)acetamido)methyl)-5,5-dimethylthiazolidine-4-carboxylic acid (Amoxicillin Impurity)
CAS:(4S)-2-(((R)-2-Amino-2-(4-hydroxyphenyl)acetamido)methyl)-5,5-dimethylthiazolidine-4-carboxylic acid (Amoxicillin Impurity)Fórmula:C15H21N3O4SPureza:98%Peso molecular:339.42(4S)-2-(((R)-2-Amino-2-(4-hydroxyphenyl)acetamido)methyl)-5,5-dimethylthiazolidine-4-carboxylic acid (Amoxicillin Impurity)
CAS:Fórmula:C15H21N3O4SPureza:98%Cor e Forma:SolidPeso molecular:339.4099Amoxicillin EP Impurity E (Mixture of Diastereomers)
CAS:Fórmula:C15H21N3O4SCor e Forma:White To Off-White SolidPeso molecular:339.41(4S)-2-[[[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino]methyl]-5,5-dimethyl-4-thiazolidinecarboxylic Acid (Mixture of Diastereomers)
CAS:Impurity Amoxicillin EP Impurity E
Applications (4S)-2-[[[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino]methyl]-5,5-dimethyl-4-thiazolidinecarboxylic Acid (Mixture of Diastereomers) (Amoxicillin EP Impurity E) is a degradation product/impurity of Amoxicillin.
References Li, Y., et al.: J. Chromat., 812, 227 (1998),Fórmula:C15H21N3O4SCor e Forma:NeatPeso molecular:339.41Amoxicillin Impurity E
CAS:(4S)-2-[[[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino]methyl]-5,5-dimethyl-4-thiazolidinecarboxylic AcidFórmula:C15H21N3O4SPureza:98%Peso molecular:339.41(4S)-2-(((R)-2-Amino-2-(4-hydroxyphenyl)acetamido)methyl)-5,5-dimethylthiazolidine-4-carboxylic acid (Amoxicillin Impurity)
CAS:Pureza:98%Peso molecular:339.41Amoxicillin EP Impurity E
CAS:Amoxicillin EP Impurity E is an impurity found in Amoxicillin EP, which is a β-lactam antibiotic. It belongs to the group of β-lactam antibiotics and has antibacterial activity. Amoxicillin EP Impurity E is found by applying validation methods to measure the concentration of this product. The analytical method used for this impurity is a wavelength measurement or a magnetic field measurement. This impurity can be determined using chromatographic or elution methods. The chromatographic methods used are high performance liquid chromatography (HPLC) and gas chromatography (GC). Method development is required for determining the level of this impurity, as well as validation procedures for measuring it with various methods.Fórmula:C15H21N3O4SPureza:Min. 95%Peso molecular:339.41 g/molRef: 3D-IA180683
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