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Merck
CN

47829

D-(+) Glucose

analytical standard

Synonym(s):

D-(+)-Glucose, Dextrose

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About This Item

Empirical Formula (Hill Notation):
C6H12O6
CAS Number:
Molecular Weight:
180.16
UNSPSC Code:
12164500
PubChem Substance ID:
EC Number:
200-075-1
Beilstein/REAXYS Number:
1724615
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grade

analytical standard

CofA

current certificate can be downloaded

packaging

pkg of 1 g

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

solubility

H2O: soluble

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

storage temp.

2-30°C

General description

Product 47829 has been discontinued. Product 47249 may be an acceptable replacement.

Storage Class

11 - Combustible Solids

wgk

WGK 1

ppe

Eyeshields, Gloves, type N95 (US)


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Dextrose as carbon source in the culture of Litopenaeus vannamei (Boone, 1931) in a zero exchange system
Suita.MS, et al.
Latin American Journal of Aquatic Research, 43(3), 2017-2017 null
NPCS board et al.
Investment Opportunity in Drugs & Pharmaceutical Projects (2013)
Ragadeepthi Tunduguru et al.
Biochemical pharmacology, 92(2), 380-388 (2014-09-10)
Skeletal muscle accounts for ∼ 80% of postprandial glucose clearance, and skeletal muscle glucose clearance is crucial for maintaining insulin sensitivity and euglycemia. Insulin-stimulated glucose clearance/uptake entails recruitment of glucose transporter 4 (GLUT4) to the plasma membrane (PM) in a
Natalia Felitsyn et al.
Journal of neurochemistry, 106(5), 2068-2079 (2008-07-31)
Delta-aminolevulinic acid (delta-ALA) is a heme precursor implicated in neurological complications associated with porphyria and tyrosinemia type I. Delta-ALA is also elevated in the urine of animals and patients treated with the investigational drug dichloroacetate (DCA). We postulated that delta-ALA
Laura C Tegtmeyer et al.
The New England journal of medicine, 370(6), 533-542 (2014-02-07)
Congenital disorders of glycosylation are genetic syndromes that result in impaired glycoprotein production. We evaluated patients who had a novel recessive disorder of glycosylation, with a range of clinical manifestations that included hepatopathy, bifid uvula, malignant hyperthermia, hypogonadotropic hypogonadism, growth

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