C4520

Cephalothin sodium salt

Manufacturer: Sigma Aldrich

CAS Number: 58-71-9

Synonym(S): 7-(2-Thienylacetamido)cephalosporanic acid sodium salt, Cephalotin sodium salt

Select a Size

Pack Size SKU Availability Price
250 MG C4520-250-MG In Stock ₹ 4,016.08
1 G C4520-1-G In Stock ₹ 9,222.90
5 G C4520-5-G In Stock ₹ 31,370.85

C4520 - 250 MG

₹ 4,016.08

In Stock

Quantity

1

Base Price: ₹ 4,016.08

GST (18%): ₹ 722.894

Total Price: ₹ 4,738.974

form

crystalline powder

Quality Level

200

antibiotic activity spectrum

Gram-negative bacteriaGram-positive bacteria

Mode of action

cell wall synthesis | interferes

storage temp.

2-8°C

SMILES string

[Na+].CC(=O)OCC1=C(N2[C@H](SC1)[C@H](NC(=O)Cc3cccs3)C2=O)C([O-])=O

InChI

1S/C16H16N2O6S2.Na/c1-8(19)24-6-9-7-26-15-12(14(21)18(15)13(9)16(22)23)17-11(20)5-10-3-2-4-25-10;/h2-4,12,15H,5-7H2,1H3,(H,17,20)(H,22,23);/q;+1/p-1/t12-,15-;/m1./s1

InChI key

VUFGUVLLDPOSBC-XRZFDKQNSA-M

Other Options

Image Product Name Manufacturer Price Range
11-102-2963
Cefalotin Sodium, British Pharmacopoeia (BP) Reference Standard, MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 26,865.84
50-178-8619
Sigma Aldrich Fine Chemicals Biosciences Cephalothin Sodium Salt | 58-71-9 | MFCD00072025 | 5g
Sigma Aldrich Fine Chemicals Biosciences ₹ 50,719.97
50-490-253
Chem-Impex International, Inc. Cephalothin sodium salt | 58-71-9 | MFCD00072025 | 1G
Chem-Impex International, Inc. ₹ 4,449.12
50-490-254
Chem-Impex International, Inc. Cephalothin sodium salt | 58-71-9 | MFCD00072025 | 5G
Chem-Impex International, Inc. ₹ 18,480.96
BP908
Cefalotin sodium
Sigma Aldrich ₹ 24,767.60
C0682000
Cefalotin sodium
Sigma Aldrich ₹ 14,267.35
Y0000505
Cefalotin for impurity B identification
Sigma Aldrich ₹ 14,072.50
C4520
Cephalothin sodium salt
Sigma Aldrich ₹ 4,016.08 - ₹ 31,370.85

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Description

  • General description: Chemical structure: ß-lactam
  • Application: Cephalothin is a first-generation cephalosporin antibiotic used to study the mechanism of liposome encapsulated antibiotics[1], strategies for co-opting β-lactamases of Gram-negative bacteria for treatment of antibiotics[2], and for immunology studies in relation to antibiotics.[3] It is used to study the effect of expression, binding and inhibition of penicillin-binding proteins especially PBP6 on bacterial cell wall mucopeptide synthesis.
  • Biochem/physiol Actions: Mode of Action: Disrupts the synthesis of the peptidoglycan layer of bacterial cell walls. Antimicrobial spectrum: Effective aginast both Gram-positive and Gram-negative bacteria. Mode of Resistance: Production of cephalosporinase will inactivate the product.
  • Other Notes: Keep container tightly closed in a dry and well-ventilated place. Keep in a dry place.

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

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form:
crystalline powder

Quality Level:
200

antibiotic activity spectrum:
Gram-negative bacteriaGram-positive bacteria

Mode of action:
cell wall synthesis | interferes

storage temp.:
2-8°C

SMILES string:
[Na+].CC(=O)OCC1=C(N2[C@H](SC1)[C@H](NC(=O)Cc3cccs3)C2=O)C([O-])=O

InChI:
1S/C16H16N2O6S2.Na/c1-8(19)24-6-9-7-26-15-12(14(21)18(15)13(9)16(22)23)17-11(20)5-10-3-2-4-25-10;/h2-4,12,15H,5-7H2,1H3,(H,17,20)(H,22,23);/q;+1/p-1/t12-,15-;/m1./s1

InChI key:
VUFGUVLLDPOSBC-XRZFDKQNSA-M

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