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Merck

1033203

USP

Ampicillinnatrium

United States Pharmacopeia (USP) Reference Standard

Synonym(e):

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

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125 MG

€ 340,00

€ 340,00


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Über diesen Artikel

Empirische Formel (Hill-System):
C16H18N3NaO4S
CAS-Nummer:
Molekulargewicht:
371.39
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4119211

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Unterstützung erhalten

SMILES string

[Na+].CC1(C)SC2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C([O-])=O

grade

pharmaceutical primary standard

API family

ampicillin

manufacturer/tradename

USP

mp

215 °C (dec.) (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

InChI

1S/C16H19N3O4S.Na/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);/q;+1/p-1/t9-,10-,11+,14-;/m1./s1

InChI key

KLOHDWPABZXLGI-YWUHCJSESA-M

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Dieser Artikel
PHR1424A01661033407
manufacturer/tradename

USP

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

USP

grade

pharmaceutical primary standard

grade

certified reference material, pharmaceutical secondary standard

grade

-

grade

pharmaceutical primary standard

format

neat

format

neat

format

-

format

neat

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

-

application(s)

pharmaceutical (small molecule)

API family

ampicillin

API family

ampicillin

API family

-

API family

ampicillin

mp

215 °C (dec.) (lit.)

mp

215 °C (dec.) (lit.)

mp

215 °C (dec.) (lit.)

mp

198-200 °C (dec.) (lit.)

General description

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Biochem/physiol Actions

Wirkungsweise: Dieses Produkt ist ein β-Lactam-Antibiotikum, das die Zellwandsynthese von Bakterien hemmt, indem es Transpeptidasen auf der Innenoberfläche der Zellmembran der Bakterien deaktiviert.

Wirkungsweise der Resistenz: Die Verabreichung zusammen mit β-Lactamase spaltet den β-Lactam-Ring von Ampicillin und deaktiviert ihn.

Antimikrobielles Spektrum: Enthält sowohl grampositive (Benzylpenicillin-ähnliche) wie auch gramnegative (Tetracyclin- und Chloramphenicol-ähnliche) Bakterien.

Analysis Note

These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.  ​

Other Notes

Sales restrictions may apply.

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

Lagerklasse

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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Lot/Batch Number

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Die Dokumentenbibliothek aufrufen

Mohamed F Mohamed et al.
PloS one, 9(12), e116259-e116259 (2015-01-01)
Staphylococcus pseudintermedius is a major cause of skin and soft tissue infections in companion animals and has zoonotic potential. Additionally, methicillin-resistant S. pseudintermedius (MRSP) has emerged with resistance to virtually all classes of antimicrobials. Thus, novel treatment options with new
Mohamed F Mohamed et al.
Antimicrobial agents and chemotherapy, 58(7), 4113-4122 (2014-05-07)
The seriousness of microbial resistance combined with the lack of new antimicrobials has increased interest in the development of antimicrobial peptides (AMPs) as novel therapeutics. In this study, we evaluated the antimicrobial activities of two short synthetic peptides, namely, RRIKA
Xukun Deng et al.
Journal of medicinal food, 17(7), 787-794 (2014-06-19)
This study investigated the active components and the anti-tumor efficacy and mechanisms of the flavonoids from Docynia delavayi (Franch.) Schneid. (DDS). MTT assay was used to examine the growth inhibitory effects of the four flavonoids, including chrysin, quercetin, naringenin, and
Michiru Nishi et al.
Journal of immunological methods, 412, 53-69 (2014-07-11)
In vitro assembly of two or three PCR fragments using primers is a common method of constructing scFv fragments for display on the surface of phage. However, mismatch annealing often occurs during in this step, leading to cloning and display
Marta Putrinš et al.
Infection and immunity, 83(3), 1056-1067 (2015-01-07)
Uropathogenic strains of Escherichia coli (UPEC) are the major cause of bacteremic urinary tract infections. Survival in the bloodstream is associated with different mechanisms that help to resist serum complement-mediated killing. While the phenotypic heterogeneity of bacteria has been shown

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