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48260

Millipore

D-(+)-galactose

suitable for microbiology, ≥99.0%

Synonyme(s) :

Galactose

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About This Item

Formule empirique (notation de Hill):
C6H12O6
Numéro CAS:
Poids moléculaire :
180.16
Numéro Beilstein :
1724619
Numéro CE :
Numéro MDL:
Code UNSPSC :
41106212
ID de substance PubChem :
Nomenclature NACRES :
NA.85

Niveau de qualité

Pureté

≥99.0% (sum of enantiomers, HPLC)
≥99.0%

Forme

powder

Activité optique

[α]20/D +80±1°, 24 hr, c = 5% in H2O

Résidus de calcination

≤0.1% (as SO4)

Perte

≤0.1% loss on drying

Pf

167-170 °C (dec.)
168-170 °C (lit.)

Solubilité

H2O: 0.1 g/mL, clear, colorless

Traces d'anions

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤50 mg/kg

Traces de cations

As: ≤0.1 mg/kg
Ca: ≤20 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

Application(s)

microbiology

Chaîne SMILES 

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

InChI

1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4+,5+,6-/m0/s1

Clé InChI

GZCGUPFRVQAUEE-KCDKBNATSA-N

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Description générale

Galactose, a member of a group of carbohydrates known as simple sugars (monosaccharides). It is usually found in nature combined with other sugars, as, for example, in lactose (milk sugar). Galactose is also found in complex carbohydrates (see polysaccharide) and in carbohydrate-containing lipids called glycolipids. It is used as a source of carbon and contributes to energy metabolism via its conversion to glucose by the enzymes that constitute the Leloir pathway. It is used in various media for the cultivation of bacteria and fungi. The metabolic steps of D-galactose utilization are catalysed by the GalK (galactokinase), GalT (galactose 1-phosphateuridylyl transferase), and GalE (UDP-galactose-4-epimerase) proteins.

Application

Galactose can be used as a carbohydrate source for diverse organisms for example lactobacilli, coliforms, Salmonella and streptococci. It is a simple monosaccharide that serves as an energy and carbon source for the cultivation of various of bacteria, fungi and yeasts in many industries such as food, pharmaceuticals and cosmetics

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Consulter la Bibliothèque de documents

Vidhya Bharathi et al.
Bio-protocol, 7(15), e2440-e2440 (2017-08-05)
The yeast Saccharomyces cerevisiae (S. cerevisiae) harboring ade1 or ade2 mutations manifest red colony color phenotype on rich yeast medium YPD. In these mutants, intermediate metabolites of adenine biosynthesis pathway are accumulated. Accumulated intermediates, in the presence of reduced glutathione
Lucia Pažitná et al.
Journal of biotechnology, 314-315, 34-40 (2020-04-17)
Glycosylation of therapeutic glycoproteins significantly affects their physico-chemical properties, bioactivity and immunogenicity. The determination of glycan composition is highly important regarding their development and production. Therefore, there is a demand for analytical techniques enabling rapid and reliable glycoprofiling of therapeutic
Alexandra Menna et al.
Bio-protocol, 10(5), e3546-e3546 (2021-03-05)
The plant cell wall is a complex network of polysaccharides and proteins that provides strength and structural integrity to plant cells, as well as playing a vital role in growth, development, and defense response. Cell wall polysaccharides can be broadly
Michelle P Christie et al.
PloS one, 9(4), e95024-e95024 (2014-04-17)
Glycosylation of biopharmaceuticals can mediate cell specific delivery by targeting carbohydrate receptors. Additionally, glycosylation can improve the physico-chemical (drug-like) properties of peptide based drug candidates. The main purpose of this study was to examine if glycosylation of the peptide enkephalin
Lu Han et al.
Biomaterials, 44, 111-121 (2015-01-27)
Multifunctional nanocomplexes (NCs) consisting of urocanic acid-modified galactosylated trimethyl chitosan (UA-GT) conjugates as polymeric vectors, poly(allylamine hydrochloride)-citraconic anhydride (PAH-Cit) as charge-reversible crosslinkers, and vascular endothelial growth factor (VEGF) siRNA as therapeutic genes, were rationally designed to simultaneously overcome the extracellular

Articles

Culture media provides a habitat with suitable nutrients, energy sources, and certain environmental conditions for the growth of microorganisms. The components of the culture media range from simple sugars to peptones, salts, antibiotics, and complex indicators.

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