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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 4800-94-6 Chemical Structure| 4800-94-6
Chemical Structure| 4800-94-6

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Carbenicillin disodium is a semi-synthetic penicillin antibiotic which interferes with cell wall synthesis of Gram-negative bacteria while displaying low toxicity.

Synonyms: Sodium carbenicillin; Carbenicillin(sodium salt); NSC 111071

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Product Details of Carbenicillin disodium

CAS No. :4800-94-6
Formula : C17H16N2Na2O6S
M.W : 422.36
SMILES Code : O=C([C@@H](C(C)(C)S[C@]1([H])[C@@H]2NC(C(C([O-])=O)C3=CC=CC=C3)=O)N1C2=O)[O-].[Na+].[Na+]
Synonyms :
Sodium carbenicillin; Carbenicillin(sodium salt); NSC 111071
MDL No. :MFCD00077683
InChI Key :RTYJTGSCYUUYAL-YCAHSCEMSA-L
Pubchem ID :20933

Safety of Carbenicillin disodium

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H317-H334
Precautionary Statements:P261-P272-P280-P284-P302+P352-P304+P340-P333+P313-P342+P311-P362+P364-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of Carbenicillin disodium

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 4800-94-6 ]

[ 4800-94-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56-95-1 ]
  • [ 4800-94-6 ]
  • chlorhexidine carbenicillin [ No CAS ]
YieldReaction ConditionsOperation in experiment
93% In water; butan-1-ol; at 20℃; for 48.0h; General procedure: The synthesis and physical characterization of four beta-lactam-based chlorhexidine GUMBOS, namely chlorhexidine di-ampicillin, chlorhexidine carbenicillin, chlorhexidine di-cephalothin and chlorhexidinedi-oxacillin, were performed using methods previously reported by Cole et al. (2013) [24], but with slight modification. Briefly, stoichiometric amounts of <strong>[56-95-1]chlorhexidine diacetate</strong> and beta-lactam antibiotic, with the latter in slight excess, was stirred for 48 h at room temperature in a butanol:water (1:1) mixture to ensure the complete formation of the beta-lactam-based chlorhexidine GUMBOS. After removing butanol from the GUMBOS products, they were purified by washing several times with cold deionized water and dried overnight with a high vacuum. The structures of chlorhexidine di-ampicillin, chlorhexidine carbenicillin, chlorhexidine di-oxacillin and chlorhexidine di-cephalothin (Figure 1) were mainly confirmed by NMR, mass spectrometry and elemental analysis, among other spectroscopic data.
 

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