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PHR1393

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Ampicillin-Trihydrat

Pharmaceutical Secondary Standard; Certified Reference Material

Synonym(e):

Ampicillin Trihydrat, D-(−)-α-Aminobenzylpenicillin

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About This Item

Empirische Formel (Hill-System):
C16H19N3O4S · 3H2O
CAS-Nummer:
Molekulargewicht:
403.45
Beilstein:
5399534
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

certified reference material
pharmaceutical secondary standard

Qualitätsniveau

Agentur

traceable to BP 785
traceable to Ph. Eur. A1000000
traceable to USP 1033000/1033407

API-Familie

ampicillin

Analysenzertifikat (CofA)

current certificate can be downloaded

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

mp (Schmelzpunkt)

198-200 °C (dec.) (lit.)

Anwendung(en)

pharmaceutical (small molecule)

Format

neat

Lagertemp.

2-8°C

SMILES String

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

InChI

1S/C16H19N3O4S.3H2O/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;;;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);3*1H2/t9-,10-,11+,14-;;;/m1.../s1

InChIKey

RXDALBZNGVATNY-CWLIKTDRSA-N

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Allgemeine Beschreibung

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.

Anwendung

Ampicillin trihydrate may be used as an analytical reference standard for the determination of ampicillin in plasma samples and pharmaceutical formulations by chromatography techniques.
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.

Biochem./physiol. Wirkung

Ein ß-Lactam-Antibiotikum mit Aminogruppen-Seitenkette an der Penicillinstruktur. Penicillin-Derivat das die bakterielle Zellwandsynthese (Peptidoglycan-Vernetzung) hemmt, indem Transpeptidasen an der inneren Oberfläche der bakteriellen Zellmembranen inaktiviert werden. Bacterizid nur für wachsende Escherichia coli . Art der Resistenz: Spaltung des β-Lactamrings des Ampicillin durch β-Lactamase. Antimikrobielles Spektrum: Gram-negative und Gram-positive Bakterien.

Fußnote

To see an example of a Certificate of Analysis for this material enter LRAA1900 in the slot below. This is an example certificate only and may not be the lot that you receive.

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Produkt-Nr.
Beschreibung
Preisangaben

Piktogramme

Health hazardExclamation mark

Signalwort

Danger

Gefahreneinstufungen

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Analysenzertifikate (COA)

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