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Merck

48260

D-(+)-Galactosa

suitable for microbiology, ≥99.0%

Sinónimos:

Galactosa

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About This Item

Fórmula empírica (notación de Hill):
C6H12O6
Número CAS:
Peso molecular:
180.16
UNSPSC Code:
41106212
NACRES:
NA.85
PubChem Substance ID:
EC Number:
200-416-4
Beilstein/REAXYS Number:
1724619
MDL number:

Nombre del producto

D-(+)-Galactosa, suitable for microbiology, ≥99.0%

InChI key

GZCGUPFRVQAUEE-KCDKBNATSA-N

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

SMILES string

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

assay

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

form

powder

optical activity

[α]20/D +80±1°, 24 hr, c = 5% in H2O

ign. residue

≤0.1% (as SO4)

loss

≤0.1% loss on drying

mp

167-170 °C (dec.)
168-170 °C (lit.)

solubility

H2O: 0.1 g/mL, clear, colorless

anion traces

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

cation traces

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

Quality Level

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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

General description

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.

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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
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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
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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
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

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