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Documenti fondamentali

PHR1772

Supelco

Meropenem

Pharmaceutical Secondary Standard; Certified Reference Material

Sinonimo/i:

Meropenem trihydrate, (1R,5S,6S)-2-[(3S,5S)-5-(dimethylaminocarbonyl)pyrrolidin-3-ylthio]-6-[(R)-1-hydroxyethyl]-1-methylcarbapen-2-em-3-carboxylic acid trihydrate

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500 MG
319,00 €

319,00 €


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Cambia visualizzazione
500 MG
319,00 €

About This Item

Formula empirica (notazione di Hill):
C17H25N3O5S · 3H2O
Numero CAS:
Peso molecolare:
437.51
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

319,00 €


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Grado

certified reference material
pharmaceutical secondary standard

Livello qualitativo

agenzia

traceable to Ph. Eur. Y0001252
traceable to USP 1392454

Famiglia di API

meropenem

CdA

current certificate can be downloaded

Confezionamento

pkg of 500 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

pharmaceutical (small molecule)

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

O.O.O.C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@@H](C3)C(=O)N(C)C)=C(N2C1=O)C(O)=O

InChI

1S/C17H25N3O5S.3H2O/c1-7-12-11(8(2)21)16(23)20(12)13(17(24)25)14(7)26-9-5-10(18-6-9)15(22)19(3)4;;;/h7-12,18,21H,5-6H2,1-4H3,(H,24,25);3*1H2/t7-,8-,9+,10+,11-,12-;;;/m1.../s1
CTUAQTBUVLKNDJ-OBZXMJSBSA-N

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Descrizione generale

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.
Meropenem belongs to the class of a semi-synthetic 1β-methylcarbapenem antibiotics. It shows an extremely broad-spectrum of antibacterial performance and is known for its high stability against renal dehydropeptidase-I (DHP-I).[1]

Applicazioni

Lincomycin Hydrochloride may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations[1][2] and peritoneal dialysis solution[3] by spectrophotometric[2] and various chromatography techniques.(58)
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Azioni biochim/fisiol

Meropenem trihydrate is an ultra-broad spectrum beta-lactam antibiotic active against both Gram-positive and Gram-negative bacteria.
Meropenem trihydrate is an ultra-broad spectrum beta-lactam antibiotic.

Risultati analitici

These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.

Altre note

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Nota a piè di pagina

To see an example of a Certificate of Analysis for this material enter LRAB7853 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

Pittogrammi

Health hazard

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Resp. Sens. 1 - Skin Sens. 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

Lot/Batch Number

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Chromatographic determination of polymerized impurities in meropenem.
Cai SY and Hu CQ
Journal of Pharmaceutical and Biomedical Analysis, 37(3), 585-589 (2005)
Ultraviolet spectrophotometry (dual wavelength and chemometric) and high performance liquid chromatography for simultaneous estimation of meropenem and sulbactam sodium in pharmaceutical dosage form.
Marwada KR, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 124(3), 292-299 (2014)
Stability of amoxycillin, clindamycin and meropenem in peritoneal dialysis solution.
Tran MD, et al.
Journal of Pharmacy Practice and Research, 42(3), 218-222 (2012)
Youngchang Kim et al.
Protein science : a publication of the Protein Society, 29(3), 723-743 (2019-12-18)
Emergence of Enterobacteriaceae harboring metallo-β-lactamases (MBL) has raised global threats due to their broad antibiotic resistance profiles and the lack of effective inhibitors against them. We have been studied one of the emerging environmental MBL, the L1 from Stenotrophomonas maltophilia
Emily Marsh et al.
Clinica chimica acta; international journal of clinical chemistry, 486, 265-268 (2018-08-18)
Therapeutic drug monitoring is used for aminoglycosides and vancomycin, and has been proposed for β-lactam antibiotics. Clinical blood samples in the ICU are often obtained via an existing vascular catheter rather than fresh needle phlebotomy. If antibiotics had previously been

Domande

1–6 di 6 domande  
  1. What concentration of Meropenem PHR1772 add in aqueous solution

    1 risposta
    1. The solubility of this product can reach 10 mg/mL in water.

      Utile?

  2. How can I determine the shelf life / expiration / retest date of this product?

    1 risposta
    1. If this product has an expiration or retest date, it will be shown on the Certificate of Analysis (COA, CofA). If there is no retest or expiration date listed on the product's COA, we do not have suitable stability data to determine a shelf life. For these products, the only date on the COA will be the release date; a retest, expiration, or use-by-date will not be displayed.
      For all products, we recommend handling per defined conditions as printed in our product literature and website product descriptions. We recommend that products should be routinely inspected by customers to ensure they perform as expected.
      For products without retest or expiration dates, our standard warranty of 1 year from the date of shipment is applicable.
      For more information, please refer to the Product Dating Information document: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/marketing/global/documents/449/386/product-dating-information-mk.pdf

      Utile?

  3. How is shipping temperature determined? And how is it related to the product storage temperature?

    1 risposta
    1. Products may be shipped at a different temperature than the recommended long-term storage temperature. If the product quality is sensitive to short-term exposure to conditions other than the recommended long-term storage, it will be shipped on wet or dry-ice. If the product quality is NOT affected by short-term exposure to conditions other than the recommended long-term storage, it will be shipped at ambient temperature. As shipping routes are configured for minimum transit times, shipping at ambient temperature helps control shipping costs for our customers. For more information, please refer to the Storage and Transport Conditions document: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/marketing/global/documents/316/622/storage-transport-conditions-mk.pdf

      Utile?

  4. I'd like to know how I can solubilize this product (Meropenem PHR1772) and what is the solubility limit. Thanks in advance.

    1 risposta
    1. Meropenem is soluble in organic solvents and aqueous solutions. It is soluble in dimethyl sulfoxide (DMSO) at a concentration of approximately 30 mg/mL.

      Utile?

  5. Hello. May I know the potency of the product Meropenem PHR1772-500mg?

    1 risposta
    1. The purity of Meropenem, product PHR1772-500mg, is batch-specific. For example, batch number LRAB7853 is 71.1% pure (mass balance); 500 mg X 0.71 = 355 mg; 355,000 ug/500 mg = 710 ug/mg.

      Utile?

  6. How should be dissolved? Storage and stability after dissolving?

    1 risposta
    1. Product PHR1772, Meropenem, is sold as a certified reference material. It is typically used as described in either the United States Pharmacopeia (USP) or the European Pharmacopoeia (EP).
      For the analysis for purity by HPLC, the USP recommends dissolving in a Triethylammonium phosphate buffer, pH 5.0; the recipe of the buffer is given in the USP. The USP goes on to recommend that the standard solution be stored in a refrigerator, and used with 24 hours.

      Utile?

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