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D-(+)-Maltose Monohidratada (1H2O) Pharmaceutical Secondary Standard - 1 Gr - Sigma

Código: 5120

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D-(+)-Maltose Monohidratada (1H2O) Pharmaceutical Secondary Standard

 

Pharmaceutical Secondary Standard; Certified Reference Material

Sinônimo(s):

D-Maltose monohydrate, 4-O-α-D-Glucopyranosyl-D-glucose, D-(+)-Maltose monohydrate, Maltobiose

Empirical Formula (Hill Notation):

C12H22O11 · H2O

Número CAS:

6363-53-7

Peso molecular:

360.31

Beilstein:

93798

Número EC:

200-716-5

Número MDL:

MFCD00149343

ID de substância PubChem:

329823418

NACRES:

NA.24

grau

certified reference material
pharmaceutical secondary standard

Nível de qualidade

300

Agency

traceable to USP 1375025

API family

maltose

Certificado de análise (CofA)

current certificate can be downloaded

embalagem

pkg of 1 g

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

pf

119-121 °C (dec.) (lit.)

application(s)

pharmaceutical (small molecule)

formato

neat

temperatura de armazenamento

2-30°C

SMILES string

O.OC[C@@H](O)[C@@H](O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@@H](O)C=O

InChI

1S/C12H22O11.H2O/c13-1-4(16)7(18)11(5(17)2-14)23-12-10(21)9(20)8(19)6(3-15)22-12;/h1,4-12,14-21H,2-3H2;1H2/t4-,5+,6+,7+,8+,9-,10+,11+,12+;/m0./s1

InChI key

HBDJFVFTHLOSDW-DNDLZOGFSA-N

Descrição geral

Maltose monohydrate is commonly used as a tablet filler or excipient in pharmaceutical industry.[1]
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.

Aplicação

Maltose Monohydrate may be used as a pharmaceutical reference standard for the determination of the analyte in drug mixtures by simulated moving bed chromatography.[2] It may also be used as a tablet filler with bisoprolol fumarate drug.[1]

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.

Nota de análise

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

Outras notas

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 de rodapé

To see an example of a Certificate of Analysis for this material enter LRAC2890 in the slot below. This is an example certificate only and may not be the lot that you receive.

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