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문서

PHR1000

Supelco

Dextrose

Pharmaceutical Secondary Standard; Certified Reference Material

동의어(들):

D-(+)-Glucose, Dextrose

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About This Item

실험식(Hill 표기법):
C6H12O6
CAS Number:
Molecular Weight:
180.16
Beilstein:
1724615
EC Number:
MDL number:
UNSPSC 코드:
12352201
PubChem Substance ID:
NACRES:
NA.24

Grade

certified reference material
pharmaceutical secondary standard

Quality Level

Agency

traceable to Ph. Eur. Y0001745
traceable to USP 1181302

API family

dextrose

분석

99.9%

CofA

current certificate can be downloaded

분석물 화학적 분류

oligosaccharides

기술

HPLC: suitable
gas chromatography (GC): suitable

mp

150-152 °C (lit.)

응용 분야

detection
food and beverages
pharmaceutical (small molecule)

형식

neat

저장 온도

2-30°C

SMILES string

OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1

InChI key

WQZGKKKJIJFFOK-DVKNGEFBSA-N

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일반 설명

Dextrose belongs to the class of sugars, and is a preferred source of carbohydrate in parenteral nutrition regimens. It is widely used in solutions to adjust tonicity, as a sweetening agent, wet granulation diluent/binder, direct-compression tablet diluent/binder, etc. It is considered only for short term clinical use, since it is deficient in electrolytes.
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.

애플리케이션

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. Dextrose has been used as a standard in the determination of additives like glucose in beverages using high performance liquid chromatography (HPLC). It may also be used as a pharmaceutical reference standard for the quantification of the analyte in pharmaceutical formulations using spectrophotometric technique.

분석 메모

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

기타 정보

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.

각주

To see an example of a Certificate of Analysis for this material enter LRAB7785 in the slot below. This is an example certificate only and may not be the lot that you receive.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

이미 열람한 고객

Determination of Additives in Beverages Using Ascentis Express Columns
Shimelis O, et al.
Sigma data, 30 (2013)
Handbook of Pharmaceutical Excipients (1986)
A multicommuted flow system for the determination of dextrose in parenteral and hemodialysis concentrate solutions
Knochen M, et al. et al.
Journal of Pharmaceutical and Biomedical Analysis, 37(4), 823-828 (2005)
Handbook of Starch Hydrolysis Products and their Derivatives (1995)
Saunders Handbook of Veterinary Drugs - E-Book: Small and Large Animal (2010)

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