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PIVAMPICILLIN

CAS No.
33817-20-8
Chemical Name:
PIVAMPICILLIN
Synonyms
mk191;PIVAPICILLIN;PIVAMPICILLIN;pivampiclillin;Pivampicillin CRS;pivaloylampicillin;PIVAMPICILLIN USP/EP/BP;pivaloyloxymethylampicillinate;PIVAMPICILLIN EPP(CRM STANDARD);ampicillinpivaloyloxymethylester
CBNumber:
CB9362547
Molecular Formula:
C22H29N3O6S
Molecular Weight:
463.55
MDL Number:
MFCD00869402
MOL File:
33817-20-8.mol
Last updated:2023-05-04 17:34:37

PIVAMPICILLIN Properties

Boiling point 679.0±55.0 °C(Predicted)
Density 1.33±0.1 g/cm3(Predicted)
solubility Practically insoluble in water, freely soluble in methanol, soluble in anhydrous ethanol. It dissolves in dilute acids.
pka pKa 7.0 (Uncertain)
FDA UNII 0HLM346LL7
ATC code J01CA02

PIVAMPICILLIN price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation CCH0003260 PIVAMPICILLIN 95.00% 33817-20-8 10MG $280.35 2021-12-16 Buy
Product number Packaging Price Buy
CCH0003260 10MG $280.35 Buy

PIVAMPICILLIN Chemical Properties,Uses,Production

Description

Pivampicillin caused sensitization in 56 workers at a penicillin factory. Pivampicillin and pivmecillinam were responsible for contact dermatitis in pharmaceutical production workers. Ampicillin, mecillinam, penicillin V and penicillin G were also implicated in cross reactions.

Chemical Properties

White or almost white, crystalline powder.

Originator

Maxifen ,Sharp and Dohme, W. Germany ,1972

Uses

Antibacterial.

Definition

ChEBI: Pivampicillin is a penicillanic acid ester that is the pivaloyloxymethyl ester of ampicillin. It is a prodrug of ampicillin. It has a role as a prodrug. It is a penicillanic acid ester and a pivaloyloxymethyl ester. It is functionally related to an ampicillin.

Manufacturing Process

(A) Pivaloyloxymethyl D(-)-α-azidobenzylpenicillinate: To a suspension of potassium D(-)α-azidobenzylpenicillinate (4.14 g) and potassium dicarbonate(1.5 g) in acetone (100 ml) and 10% aqueous sodium iodide (2 ml), chloromethyl pivalate (2.7 ml) was added and the mixture refluxed for 2 hours. After cooling, the suspension was filtered and the filtrate evaporated to dryness in vacuo. The remaining residue was washed repeatedly by decantation with petroleum ether to remove unreacted chloromethyl pivalate. The oily residue was taken up in ethyl acetate (100 ml), and the resulting solution washed with aqueous sodium bicarbonate and water, dried and evaporated in vacuo to yield the desired compound as a yellowish gum, which crystallized from ether, melting point 114°C to 115°C.
(B) Pivaloyloxymethyl D(-)-α-aminobenzylpenicillinate, hydrochloride: To a solution of pivaloyloxymethyl D(-)-α-azidobenzylpenicillinate (prepared as described above) in ethyl acetate (75 ml) a 0.2 M phosphate buffer (pH 2.2) (75 ml) and 10% palladium on carbon catalyst (4 g) were added, and the mixture was shaken in a hydrogen atmosphere for 2 hours at room temperature. The catalyst was filtered off, washed with ethyl acetate (25 ml) and phosphate buffer (25 ml), and the phases of the filtrate were separated. The aqueous phase was washed with ether, neutralized (pH 6.5 to 7.0) with aqueous sodium bicarbonate, and extracted with ethyl acetate (2 x 75 ml). To the combined extracts, water (75 ml) was added, and the pH adjusted to 2.5 with 1 N hydrochloric acid. The aqueous layer was separated, the organic phase extracted with water (25 ml), and the combined extracts were washed with ether, and freeze-dried. The desired compound was obtained as a colorless, amorphous powder.
The purity of the compound was determined iodometrically to be 91%. A crystalline hydrochloride was obtained from isopropanol with a melting point of 155°C to 156°C (dec.).

Therapeutic Function

Antibacterial

Contact allergens

Pivampicillin is a prodrug of ampicillin. It caused sensitization in 56 workers at a penicillin factory. Pivampicillin and pivmecillinam were responsible for contact dermatitis in pharmaceutical production workers. Ampicillin, mecillinam or amdinocillin, penicillin V and penicillin G were also implicated in cross-reactions.

PIVAMPICILLIN Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 39)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-18789408387 1057@dideu.com China 3684 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9456 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29321 58
Guangzhou PI PI Biotech Inc +86-020-81716320 +86-13602409664 Sales@pipitech.com China 3635 55
Beijing HuaMeiHuLiBiological Chemical 010-56205725 waley188@sohu.com China 12338 58
Shanghai T&W Pharmaceutical Co., Ltd. +86 21 61551611 China 9901 58
ChemStrong Scientific Co.,Ltd 0755-66853366 13670046396 sales@chem-strong.com China 17982 56
Alta Scientific Co., Ltd. 022-6537-8550 15522853686 sales@altasci.com.cn China 4515 55
BOC Sciences 16314854226 info@bocsci.com United States 9926 65

View Lastest Price from PIVAMPICILLIN manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
PIVAMPICILLIN USP/EP/BP pictures 2021-06-28 PIVAMPICILLIN USP/EP/BP
33817-20-8
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
PivaMpicillin  pictures 2020-05-12 PivaMpicillin
33817-20-8
US $1.00 / KG 1KG 99% 20T Shaanxi Dideu Medichem Co. Ltd
  • PivaMpicillin  pictures
  • PivaMpicillin
    33817-20-8
  • US $1.00 / KG
  • 99%
  • Shaanxi Dideu Medichem Co. Ltd
4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylicacid,6-(2-amino-2-phenylacetami ampicillinpivaloyloxymethylester hydroxymethylester,pivalate(ester),d-(-)-do)-3-dimethyl-7-oxo- mk191 pivaloylampicillin pivaloyloxymethylampicillinate PIVAMPICILLIN PIVAPICILLIN pivampiclillin 6α-[[(R)-Aminophenylacetyl]amino]penicillanic acid (2,2-dimethyl-1-oxopropoxy)methyl ester PIVAMPICILLIN EPP(CRM STANDARD) (2S,5R,6R)-6-(((2R)-Aminophenylacetyl)amino)3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid Pivampicillin CRS 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, (2S,5R,6R)- (2S,5R,6R)-(pivaloyloxy)methyl 6-((R)-2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate PIVAMPICILLIN USP/EP/BP 33817-20-8 C22H29N3O6S