Saltar al contenido
MilliporeSigma
Todas las fotos(1)

Key Documents

SMB00608

Sigma-Aldrich

Potassium clavulanate: silicon dioxide (1:1)

Sinónimos:

Potassium clavulanate: silicon dioxide

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

UNSPSC Code:
12352200

form

powder

color

off-white

solubility

water: 1 mg/mL, clear to slightly hazy

antibiotic activity spectrum

Gram-negative bacteria
Gram-positive bacteria

mode of action

enzyme | inhibits

storage temp.

2-8°C

General description

Material is a powdered mixture of 1 part potassium clavulanate to 1 part silicon dioxide.

Biochem/physiol Actions

Clavulanate is a β-lactam antibiotic related to the penicillins. Clavulanate competitively and irreversibly inhibits a wide variety of β-lactamases found in bacteria that are resistant to penicillins and cephalosporins.

Packaging

1G

Storage and Stability

Keep container tightly closed in a dry and well-ventilated place. Never allow produc to get in contact with water during storage.

Other Notes

Keep container tightly closed in a dry and well-ventilated place. Never allow product to get in contact with water during storage.

pictograms

FlameHealth hazard

signalword

Danger

Hazard Classifications

Resp. Sens. 1 - Self-heat. 2 - Skin Sens. 1 - STOT RE 1 Inhalation

target_organs

Lungs

supp_hazards

Storage Class

4.2 - Pyrophoric and self-heating hazardous materials

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

B G Spratt et al.
Antimicrobial agents and chemotherapy, 12(3), 406-409 (1977-09-01)
Thienamycin and clavulanic acid are new beta-lactam derivatives with structures markedly different from those of penicillins or cephalosporins. Both derivatives had the same general mode of action as typical beta-lactam antibiotics since they bound to precisely the same proteins as
C Reading et al.
Antimicrobial agents and chemotherapy, 11(5), 852-857 (1977-05-01)
A novel beta-lactamase inhibitor has been isolated from Streptomyces clavuligerus ATCC 27064 and given the name clavulanic acid. Conditions for the cultivation of the organism and detection and isolation of clavulanic acid are described. This compound resembles the nucleus of

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico