N-Pivaloyl Amoxicillin

Chemical Name N-Pivaloyl Amoxicillin
Alternate Names Amoxicillin Impurities, Impurities of Amoxicillin
CAT No. CS-T-03710
CAS Registry# 1313237-94-3
Category Impurities
Stock IN-Stock
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Amoxicillin
Therapeutic Anti ulcer
Canonical Smiles CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=C(C=C3)O)NC(=O)C(C)(C)C)C(=O)O)C
InchIKey SEPXWAZZCPMULA-VWPFQQQWSA-N
Inchl InChI=1S/C21H27N3O6S/c1-20(2,3)19(30)23-12(10-6-8-11(25)9-7-10)15(26)22-13-16(27)24-14(18(28)29)21(4,5)31-17(13)24/h6-9,12-14,17,25H,1-5H3,(H,22,26)(H,23,30)(H,28,29)/t12-,13-,14+,17-/m1/s1
IUPAC (2S,5R,6R)-6-[[(2R)-2-(2,2-dimethylpropanoylamino)-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Controlled No
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N-Pivaloyl Amoxicillin, also known as PivAmox, is a prodrug of Amoxicillin, which is widely used to treat bacterial infections. PivAmox is a semi-synthetic derivative of Amoxicillin, meaning it is chemically modified to enhance its pharmacological properties. PivAmox is commonly used in the pharmaceutical industry for the production of oral dosage forms such as tablets, capsules, and suspensions. It is used to treat a wide range of bacterial infections, including respiratory tract infections, urinary tract infections, skin infections, and ear infections. The chemical structure of PivAmox consists of a β-lactam ring, which is responsible for its antibacterial activity. The β-lactam ring inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins (PBPs) in the bacterial cell membrane, leading to cell death. PivAmox is a white crystalline powder with a molecular weight of 419.5 g/mol. It is insoluble in water but soluble in organic solvents such as methanol, ethanol, and acetone. PivAmox has a melting point of 118-120°C and a boiling point of 460.7°C at 760 mmHg. In conclusion, PivAmox is a prodrug of Amoxicillin that is widely used in the pharmaceutical industry to treat bacterial infections. Its chemical structure consists of a β-lactam ring, which is responsible for its antibacterial activity. PivAmox is insoluble in water but soluble in organic solvents and has a melting point of 118-120°C.

Related Compounds

Amoxicillin EP Impurity H | Amoxicillin EP Impurity B | N-(Hydroxyphenylglycyl) amoxicillin Sodium salt | Amoxicillin EP Impurity O | Amoxicillin Impurity C (R Isomer) | Amoxicillin Close ring Trimer | p-hydroxyphenylglycine methyl ester | Amoxicillin Trimer | Amoxicillin oxide | Amoxicillin EP Impurity K trisodium salt | Amoxicillin EP Impurity C | Amoxicillin EP Impurity K | Amoxicillin double Side Chain Impurity | Amoxicillin Open Ring Trimer Impurity | Amoxicillin Open RIng Trimer Impurity sodium salt | Amoxicillin Dimer (Penicilloic acid form) | Amoxicillin Open Ring Ethyl | Amoxicillin EP Impurity P | rac-Amoxicillin EP Impurity H | Amoxicillin Related Compound D | Amoxicillin EP Impurity J Disodium salt | Amoxicillin Impurity M | Amoxicillin Related Compound M | Amoxicillin Related Compound E | Amoxicillin Trihydrate - Impurity J | Amoxicillin Open Ring Decarboxylated Dimer | Amoxicillin EP Impurity L | Amoxicillin EP Impurity F | Amoxicilloic Acid | Sterile Clavulanate Potassium+Amoxicillin | Amoxicillin EP Impurity H | Amoxicillin Trihydrate - Impurity K | Amoxicillin Trimer Trisodium Salt | Amoxicillin Aldehyde | Amoxicilline EP Impurity D (Mixture of isomers) | Amoxicillin EP Impurity I | Amoxicillin Related Compound C | Amoxicillin Related Compound M Sodum salt | Amoxicillin EP Impurity J | N-Nitroso Amoxicillin |

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