ChemicalBook >> CAS DataBase List >>Potassium clavulanate

Potassium clavulanate

CAS No.
61177-45-5
Chemical Name:
Potassium clavulanate
Synonyms
CLAVULANATE POTASSIUM;Clavulanate;Potassium Clavulanat;potassium calvulanate;Potassium clavulanate USP/EP/BP;MM 1415;Amonate;brl14151k;Clavulanate K;CLAVULANTE POTASSIUM
CBNumber:
CB2722502
Molecular Formula:
C8H10KNO5
Molecular Weight:
239.27
MDL Number:
MFCD01710901
MOL File:
61177-45-5.mol
Last updated:2024-04-22 13:28:10

Potassium clavulanate Properties

Melting point >1600C (dec)
alpha +55~+60°
storage temp. Inert atmosphere,2-8°C
solubility Freely soluble in water, slightly soluble in ethanol (96 per cent), very slightly soluble in acetone.
InChIKey ABVRVIZBZKUTMK-JSYANWSFSA-M
CAS DataBase Reference 61177-45-5(CAS DataBase Reference)
FDA UNII Q42OMW3AT8

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS08
Signal word  Danger
Hazard statements  H228-H252-H317-H334
Precautionary statements  P210-P235-P280-P302+P352-P304+P340+P312-P403+P235
Hazard Codes  F,Xn,Xi
Risk Statements  11-42/43-44-36-14
Safety Statements  8-16-22-36/37-45-43-26
RIDADR  UN1325 - class 4.1 - PG 2 - Flammable solids, organic, n.o.s., HI: all
WGK Germany  2
RTECS  RN6802700
HS Code  2941900000
NFPA 704
4
0 0

Potassium clavulanate price More Price(26)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 33454 Potassium clavulanate VETRANAL 61177-45-5 100mg $199 2024-03-01 Buy
Cayman Chemical 19456 Clavulanate (potassium salt) ≥95% 61177-45-5 5mg $29 2024-03-01 Buy
Cayman Chemical 19456 Clavulanate (potassium salt) ≥95% 61177-45-5 10mg $51 2024-03-01 Buy
Cayman Chemical 19456 Clavulanate (potassium salt) ≥95% 61177-45-5 25mg $78 2024-03-01 Buy
Cayman Chemical 19456 Clavulanate (potassium salt) ≥95% 61177-45-5 50mg $99 2024-03-01 Buy
Product number Packaging Price Buy
33454 100mg $199 Buy
19456 5mg $29 Buy
19456 10mg $51 Buy
19456 25mg $78 Buy
19456 50mg $99 Buy

Potassium clavulanate Chemical Properties,Uses,Production

Description

Potassium clavulanate is a semi-synthetic beta-lactamase inhibitor isolated from Streptomyces. The compound contains a beta-lactam ring and strongly binds to beta-lactamase at their new active site, which protects other beta-lactam antibiotics such as amoxicillin from beta-lactamase catalysis.

Uses

Combination of potassium clavulanate and amoxicillin is normally used in medicine to treat numerous different infections caused by bacteria, for instance, pneumonia, sinusitis, ear infections, urinary tract infections, bronchitis, and skin infections. Potassium clavulanate can also combined with other penicillin-based antibiotics.

Cautions

Before taking a combination of potassium clavulanate with any other penicillin-based antibiotic, one should discuss with medical providers and let them know whether they have severe kidney disease, jaundice or liver problems. In addition, it is important to inform the physician if an individual is allergic to penicillin or cephalosporin antibiotic, such as Amoxil, Levaquin, omnicef, and cefzil.

Although it is not clear with this drug may harm an unborn baby, it is important to inform the physician if one is pregnant or intending to become pregnant. In addition, studies have indicated that pass into breast milk, thus may affect a nursing infant. As such, it is important to inform the doctor if one is breast-feeding. Children should never be given potassium clavulanate without consulting a physician.

Administration

The drug should be take according to the prescription given by the doctor. Potassium clavulanate is taken orally every 12 hours at the start of a meal to minimize side effects such as stomach upset.

The extended release of the potassium clavulanate tablet must never been chewed or crushed. The medicine should be swallowed as a whole while the chewable tablet must be chewed before swallowing it. Before measuring a dose, the liquid medicine must be shaken well. The medicine should be only used for the full length of prescribed time. It is important not to skip any doses as it may lead to further infection that is resistant to antibiotics.

The medicine should never be taken with or just after ingesting a high-fat meal as it will make it harder for the body to absorb the drug.

Side Effects

Potassium clavulanate may cause diarrhea that is bloody or watery when taken in combination with amoxicillin. It may also lead to severe stomach pain, swelling of the face or tongue, loss of appetite, fever, dark color urine, weakness, or confusion. The medicine may cause jaundice or yellowing of skin as well as vaginal itching or discharge.

Description

Clavulanate is a β-lactamase inhibitor that is effective against Ambler class A β-lactamases (IC50 values range from 12 to 60 nM). While it is not an effective antibiotic by itself, clavulanate is commonly used with other antibiotics that would be inactivated by β-lactamases secreted by bacteria. It is often combined with amoxicillin and other penicillin-based antibiotics.

Chemical Properties

Pale Yellowish Solid

Originator

Clavulanate ,potassium Lek

Uses

Clavulanic acid is a β-lactam antibiotic produced by several species of Streptomyces. The free acid degrades and is isolated and maintained as either the sodium or potassium salt. Clavulanate is a weak antibiotic, but is a potent inhibitor of β-lactamases. In combination with penicillin and cephalosporins, it shows potent synergistic activity. Clavulanic acid is a suicide inhibitor, covalently binding to a serine residue in the active site of the β-lactamase.

Uses

Clavulanic Acid is a β-lactamase inhibitor, typically added to amoxicillin to increase its effectiveness.

Uses

A -Lactamase inhibitor, typically added to amoxicillin to increase its effectiveness

Definition

ChEBI: A potassium salt having clavulanate as the counterion. It acts as a suicide inhibitor of bacterial beta-lactamase enzymes and has only weak anitbiotic activity when administered alone. However it can be used in combination with amoxicillin trihydrate (under the trade name Augmentin) for treatment of a variety of bacterial infections, where it prevents antibiotic inactivation by microbial lactamases.

Manufacturing Process

Clavulanic acid may be obtained by aerobic cultivation of Streptomyces clavuligerus in conventional nutrient media at, for example, about 25°-30°C under roughly neutral conditions.
Cultivation of Streptomyces clavuligeru: Streptomyces clavuligerus was cultivated at 26°C on agar slopes containing 1% Yeatex (yeast extract) ("Yeatex" is a Registered Trade mark), 1% glucose and 2% Oxoid agar No. 3, pH 6.8. A sterile loop was used to transfer mycelium and spores from the slope into 100 ml of a liquid medium in a 500 ml Ehrlenmeyer flask. The liquid medium had the following composition: Oxoid Malt Extract 10g/L, Oxoid Bacteriological Peptone 10g/L, Glycerol 20 g/L, Tap water 1 L.
The medium was adjusted to pH 7.0 with sodium hydroxide solution and 100 ml volumes dispensed into flasks which were closed with foam plugs prior to autoclaving at 15 lb/sq.in. for 20 min. An inoculated seed flask was shaken for 3 days at 26°C on a rotary shaker with a 2 inch throw and a speed of 240 r.p.m.
Production stage flasks containing the liquid medium described above were inoculated with 5% vegetative inoculum and grown under the same conditions as the seed flask.
Clavulanic acid may be extracted from the culture medium. Normally the cells of the Streptomyces clavuligerus are first removed from culture medium by filtration or centrifugation. Then clavulanic acid is extracted into an organic solvent, for example, n-butanol or ethyl acetate, or n-butyl acetate, or methyl isobutyl ketone. Then n-butanol fraction are treated with new aqueous phase using potassium hydrogen carbonate and then this aqueous phase is washed with n-butanol. This aqueous extract, after separation of the phases, is concentrated under reduced pressure. Freeze-drying at -20°C may also be
employed to provide a solid crude preparation of the potassium Z-(2R,5R)-3- (β-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3,2,0]heptane-2-carboxylate (clavulanate potassium).

Therapeutic Function

Beta-lactamase inhibitor

Potassium clavulanate Preparation Products And Raw materials

Global( 277)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Mojin Biotechnology Co., Ltd
+8613288715578 sales@hbmojin.com China 12456 58
Sinoway Industrial co., ltd.
0592-5800732; +8613806035118 xie@china-sinoway.com China 992 58
Henan Bao Enluo International TradeCo.,LTD
+86-17331933971 +86-17331933971 deasea125996@gmail.com China 2503 58
Zibo Hangyu Biotechnology Development Co., Ltd
+86-0533-2185556 +8617865335152 Mandy@hangyubiotech.com China 11013 58
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 7845 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+8618740459177 sarah@tnjone.com China 893 58
Ouhuang Engineering Materials (Hubei) Co., Ltd
+8617702722807 admin@hbouhuang.com China 2259 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9348 55
Hubei XinRunde Chemical Co., Ltd.
+8615102730682 bruce@xrdchem.cn CHINA 566 55

View Lastest Price from Potassium clavulanate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Clavulanate potassium pictures 2024-04-22 Clavulanate potassium
61177-45-5
US $15.00 / kg 1kg 99.912% 10ton Ouhuang Engineering Materials (Hubei) Co., Ltd
Clavulanate Potassium pictures 2024-04-22 Clavulanate Potassium
61177-45-5
US $120.00-55.00 / Kg/Bag 1Kg/Bag 0.99 20 tons Sinoway Industrial co., ltd.
Potassium Clavulanate pictures 2024-04-12 Potassium Clavulanate
61177-45-5
US $0.00 / kg 1kg 99% 10000kg Shaanxi TNJONE Pharmaceutical Co., Ltd
CLAVULANIC ACID POTASSIUM CLAVULANIC ACID POTASSIUM SALT CLAVULANTE POTASSIUM MM 1415 4-Oxa-1-azabicyclo3.2.0heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, monopotassium salt, (2R,3Z,5R)- POTASSIUMCLAVULANATE,EP 4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, monopotassium salt, (2R,3Z,5R)- (9CI) 4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, monopotassium salt, [2R-(2a,3Z,5a)]- clavulanate,potassium salt CLAVULANIC ACID POTASSIUM SALT (POTASSIUM CLAVULANATE)/AVICEL (1:1) Clavulanate K Clavulanic acid potassium salt (Potassium Clavulanate)/Avicel (1 Clavulanate:Cellulose Clavulanic acid Potassium salt:Cellulose (1:1) Clavulanate PotassiuMAvicel API CLAVULANATE POTASSIUM +AVICE potassiuM (2R,5R,Z)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylate ClavubactaM potassiuM, BRL 14151 Clavullinate PotassiuM USP Microcrystalline cellulose (1:1) potassium clavulanate sterile POTASSIUM CLAVULANATE potassium (z)-(2r,5r)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylate brl14151k monopotassiumsalt,(2r-(2-alpha,3z,5-alpha))-xo CLAVULANIC POTASSIUM potassium [2R-(2alpha,3Z,5alpha)]-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylate POTASSIUM CLAVULANATE FROM STREPTOMYCES 4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, potassium salt (1:1), (2R,3Z,5R)- Amonate Clavaulanate Potassium with Microcrystalline Cellulose 1:1 Amoxicillin with Clavulanate Potassium 4:1 Trihydrate with Clavanate Potassium 4:1 Potassium Clavulanate Standard Sterile Clavulanate Potassium+Amoxicillin Clavulanate potassiumQ: What is Clavulanate potassium Q: What is the CAS Number of Clavulanate potassium Q: What is the storage condition of Clavulanate potassium Q: What are the applications of Clavulanate potassium CLAVULANATE POTASSIUM Potassium Clavulanat Clavulanate potassium calvulanate Potassium clavulanate USP/EP/BP 2,2′-(oxybismethylene)bis[2-(hydroxymethyl)propane-1,3-diol]hexanitrate(dipentaerythritylhexanitrate). Amoxicillin and Clavulanate Potassium: 1: 1 61177-45-5 C8H8NO5K C8H8KNO5 Antibiotics Antibiotics A to Z Antibiotics N-S BioChemical antibiotic Antibiotic Explorer Inhibitors Intermediates & Fine Chemicals Pharmaceuticals Pharma Amines Heterocycles