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17778

Millipore

Ticarcillin Supplement

suitable for microbiology

Synonym(s):

Ticarcillin

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About This Item

Empirical Formula (Hill Notation):
C15H16N2O6S2
CAS Number:
Molecular Weight:
384.43
EC Number:
MDL number:
UNSPSC Code:
41171614
PubChem Substance ID:
NACRES:
NA.85

Agency

according to ISO 10273:2017

Quality Level

sterility

sterile

form

powder

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental
food and beverages

microbiology

storage temp.

2-8°C

suitability

Yersinia spp.

SMILES string

CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](C(O)=O)c3ccsc3)C(=O)N2[C@H]1C(O)=O

InChI

1S/C15H16N2O6S2/c1-15(2)9(14(22)23)17-11(19)8(12(17)25-15)16-10(18)7(13(20)21)6-3-4-24-5-6/h3-5,7-9,12H,1-2H3,(H,16,18)(H,20,21)(H,22,23)/t7-,8-,9+,12-/m1/s1

InChI key

OHKOGUYZJXTSFX-KZFFXBSXSA-N

Application

An antibiotic supplement recommended for the selective enrichment of Yersinia enterocolitica.

Components

Composition (per vial; sufficient for 1000 mL medium): Ticarcillin 1.00 mg

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Pierre-François Laterre et al.
The Journal of antimicrobial chemotherapy, 70(3), 891-898 (2014-11-30)
The growing incidence of infections caused by Enterobacteriaceae producing ESBLs has led to increased use of carbapenems. Temocillin, which resists most β-lactamases, may be a useful alternative. The aim of this study was to assess the pharmacokinetics and target attainment
Anita Umerska et al.
Biomolecules, 8(4) (2018-10-27)
The worldwide occurrence of resistance to standard antibiotics and lack of new antibacterial drugs demand new strategies to treat complicated infections. Hence, the aim of this study was to examine the antibacterial activities of an antimicrobial peptide, arenicin-3 derivative AA230
Yu-Ting Liao et al.
Antimicrobial agents and chemotherapy, 58(7), 3983-3990 (2014-05-07)
The role of carbapenem-resistant Acinetobacter baumannii (CRAb) in polymicrobial infection remains elusive. Having observed the ability of CRAb to shelter other susceptible bacteria from carbapenem killing, we sought to determine the factors contributing to this sheltering effect by transforming different
Caleb J P Economou et al.
International journal of antimicrobial agents, 56(3), 106058-106058 (2020-06-27)
To describe the adsorption of ticarcillin and piperacillin on to polyethersulfone (PES) membranes using the recirculation function on an ex-vivo renal replacement circuit. Low (4-8 mg) or high (35-45 mg) doses of ticarcillin and low (4-8 mg) or high (70-80
Rémy A Bonnin et al.
Antimicrobial agents and chemotherapy, 56(7), 3923-3927 (2012-04-18)
Acinetobacter bereziniae (formerly Acinetobacter genomospecies 10) isolate Nec was recovered from a skin sample of a patient hospitalized in Paris, France. It was resistant to penicillins, penicillin-inhibitor combinations, and carbapenems. Cloning and expression in Escherichia coli identified the carbapenem-hydrolyzing class

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