Ampicillin Sodium Salt

CAS: 69-52-3

Ref. TR-A634315

Produktinformation

• Name: Ampicillin Sodium Salt
• Synonyme: Piperacillin Sodium Imp. A (EP), Piperacillin Imp. A (EP), Ampicillin Sodium, Piperacillin Sodium Imp. A (EP) as Sodium Salt, Piperacillin Imp. A (EP) as Sodium Salt, (2S,5R,6R)-6-[[(2R)-Aminophenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid monosodium salt, D-(-)-6-(2-Amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid monosodium salt, [2S-[2alpha,5alpha,6beta(S*)]]-6-[(Aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid monosodium salt, Alpen N, Amcill S, Ampi-Dry 5000, Ampicillin sodium, Ampicillin-Na, Ampicin, Anhypen, Binotal sodium, Britapen injection, Cilleral, D-alpha-Aminobenzylpenicillin sodium salt, Monosodium ampicillin, Omnipen N, Pen A/N, Penbritin S, Pentrex, Polycillin N, Principen N, Sodium 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate, Sodium 6-[D-alpha-aminophenylacetamido]penicillanoate, Sodium D-alpha-aminobenzylpenicillanate, Sodium P-50, Sodium ampicillin, Sodium ampicillinate, Sodium binotal, Solampi, Piperacillin Impurity A, Piperacillin Impurity A as Sodium Salt, Piperacillin Sodium Impurity A as Sodium Salt, Sultamicillin Impurity C as Sodium Salt, Sultamicillin Tosilate Dihydrate Impurity B as Sodium Salt, Sultamicillin Impurity B as Sodium Salt, Piperacillin Impurity A as Sodium Salt, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-, monosodium salt, <span class="text-smallcaps">D</span>-(-)-, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-, monosodium salt, [2S-[2α,5α,6β(S*)]]-, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-, sodium salt (1:1), (2S,5R,6R)-, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-aminophenylacetyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, (2S,5R,6R)-, 4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-, sodium salt, (2S,5R,6R)- (1:1), 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-,sodiumsalt,d-(-)-4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid, <span class="text-smallcaps">D</span>-α-Aminobenzylpenicillin sodium salt, Alpen-n, Amcill-s, Ampicillin Sodium oral, Ampicillin Sodium, Sterile Usp, Ampicillin, Sodium Salt, Binotalsodium, Citteral, D-(-)-Alpha-Aminobenzylpenicillin Sodium Salt, D-6-(-Amino-phenylacetamido)penicillanicacidsodiumsalt, Domicillin, Omnipen-N, Pamecil, Sodium 6-[<span class="text-smallcaps">D</span>-α-aminophenylacetamido]penicillanoate, Sodium 6-{[Amino(Phenyl)Acetyl]Amino}-3,3-Dimethyl-7-Oxo-4-Thia-1-Azabicyclo[3.2.0]Heptane-2-Carboxylate, Sodium <span class="text-smallcaps">D</span>-α-aminobenzylpenicillanate, Sodium [2S-[2Alpha,5Alpha,6Beta(S*)]]-6-(Aminophenylacetamido)-3,3-Dimethyl-7-Oxo-4-Thia-1-Azabicyclo[3.2.0]Heptane-2-Carboxylate, Totacillin N, sodium (2S,5R,6R)-6-{[(2R)-2-amino-2-phenylacetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate, sodium (2S,5R,6R)-6-{[amino(phenyl)acetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate

Beschreibung

Applications Sodium Salt of Ampicillin, an orally active, semi-synthetic antibiotic; structurally related to penicillin. Antibacterial.
References Ivashkiv, E., et al.: Anal. Profiles Drug Subs., 2, 1 (1973), Campoli-Richards, D.M., et al.: Drugs, 33, 577 (1987), Sill, M. L., et al.: Antimicrob. Agents Chemother., 52, 1551 (2008),

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 371.39
• Formel: C₁₆H₁₈N₃O₄S·Na
• Farbe/Form: Off-White
• InChl: InChI=1S/C16H19N3O4S.Na/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);/q;+1/p-1/t9-,10-,11+,14-;/m1./s1
• InChI Key: InChIKey=KLOHDWPABZXLGI-YWUHCJSESA-M
• SMILES: CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)O[Na]