C1389

Carbenicillin disodium salt

89.0-100.5% anhydrous basis

Manufacturer: Sigma Aldrich

CAS Number: 4800-94-6

Synonym(S): Carbenicillin, Disodium carbenicillin, α-Carboxybenzylpenicillin disodium salt

Select a Size

Pack Size SKU Availability Price
250 MG C1389-250-MG In Stock ₹ 6,310.98
1 G C1389-1-G In Stock ₹ 19,084.48
5 G C1389-5-G In Stock ₹ 72,246.05
10 G C1389-10-G In Stock ₹ 92,261.48

C1389 - 250 MG

₹ 6,310.98

In Stock

Quantity

1

Base Price: ₹ 6,310.98

GST (18%): ₹ 1,135.976

Total Price: ₹ 7,446.956

biological source

synthetic (chemical)

Quality Level

200

Assay

89.0-100.5% anhydrous basis

form

powder

color

white to off-white

solubility

H2O: 50 mg/mL

antibiotic activity spectrum

Gram-negative bacteriaGram-positive bacteria

Mode of action

cell wall synthesis | interferes

storage temp.

2-8°C

SMILES string

[Na+].[Na+].CC1(C)S[C@@H]2[C@H](NC(=O)C(C([O-])=O)c3ccccc3)C(=O)N2[C@H]1C([O-])=O

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Description

  • General description: Carbenicillin is a semi-synthetic, broad-spectrum carboxypenicillin antibiotic with bactericidal and beta-lactamase resistant activity. It is a broad-spectrum antibiotic, meaning that it is effective against a wide range of bacteria, including both Gram-positive and Gram-negative bacteria. Carbenicillin is particularly useful against Pseudomonas aeruginosa, a Gram-negative bacterium that is often resistant to other antibiotics.Carbenicillin is commonly used in cell biology applications to prevent the growth of bacterial contaminants. It is also used in microbiology to select for bacteria that have been transformed with a vector harboring the gene encoding beta-lactamase, which makes them resistant to carbenicillin.
  • Application: Carbenicillin disodium salt has been used: in the preparation of Luria-Bertani (LB) agar plates and media[1]as a selective agent in the culture media to prevent the growth of bacterial contaminants[2] in a study focused on the development of monoclonal antibodies[3]
  • Biochem/physiol Actions: Carbenicillin acylates the penicillin-sensitive transpeptidase C-terminal domain by opening the lactam ring. This inactivation prevents the cross-linkage of peptidoglycan strands, thereby inhibiting the third and last stage of bacterial cell wall synthesis. This leads to incomplete bacterial cell wall synthesis and eventually causes cell lysis.
  • Features and Benefits: Broad-spectrum antibiotic with bactericidal and beta-lactamase resistant activityEffective against a wide range of bacteria, including Pseudomonas aeruginosaCommonly used in Cell Biology and Biochemical applicationsOffers greater stablility than ampicillin
  • Storage and Stability: Tightly closed. Dry. Keep locked up or in an area accessible only to qualified or authorized
  • Analysis Note: Stable at 37 °C for 3 days
  • Other Notes: For additional information on our range of Biochemicals, please complete this form.

SAFETY INFORMATION

Pictograms

GHS08

Signal Word

Danger

Hazard Statements

H317,H334

Precautionary Statements

P261 - P272 - P280 - P284 - P302 + P352 - P333 + P313

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves