Dextrose CAS#50-99-7

CAS: 50-99-7

MF: C6H12O6

MW: 180.16

EINECS: 200-075-1

MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)


Product Details

Dextrose CAS#50-99-7

glucose ,a short form of dextrorotatory glucose, is a stereoisomer of glucose molecule, which is biologically active and whose bottom chiral carbon has its hydroxyl group (OH) located spatially to the right. Its molecule can exist in an open-chain (acyclic) and ring (cyclic) form and has two isomers α- and β-. It is the main source of energy in the form of ATP for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. In animals, it arises from the breakdown of glycogen in a process known as glycogenolysis. D-(+)-Glucose has been used as a standard for the estimation of total sugar in hydrolyzed starch by phenol-sulfuric acid method. It has also been used in the preparation of the liquid media for culturing some yeast cells. In addition, it is used therapeutically in fluid and nutrient replacement, such as glucose syrup and glucose powder. It can be obtained by enzymatic cleavage of starch, so there are multiple sources like sugar cane, sugar beet, corn (corn syrup), potatoes and wheat. Today, large-scale starch hydrolysis is used to produce glucose.

Dextrose  Chemical Properties
Melting point 150-152 °C(lit.)
alpha 52.75 º (c=10, H2O, NH4OH 25 ºC)
Boiling point 232.96°C (rough estimate)
density 1.5440
bulk density630kg/m3
refractive index 53 ° (C=10, H2O)
storage temp. room temp
solubility H2O: 1 M at 20 °C, clear, colorless
pkapKa 12.43(H2O,t = 18,)(Approximate)
form Crystalline Powder
color White
PH5.0-7.0 (25℃, 1M in H2O)
OdorOdorless
PH Range5.9
biological sourcewheat
Optical Rotation[α]25/D +52.5 to +53.0°(lit.)
Water Solubility Soluble
λmaxλ: 260 nm Amax: 0.03
λ: 280 nm Amax: 0.02
Merck 14,4459
BRN 1281608
Henry's Law Constant7.8×108 mol/(m3Pa) at 25℃, Qin et al. (2021)
Stability:Stable. Substances to be avoided include strong oxidizing agents. Combustible.
Cosmetics Ingredients FunctionsHUMECTANT
InChI1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
InChIKeyWQZGKKKJIJFFOK-DVKNGEFBSA-N
SMILESOC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
LogP-2.490 (est)
CAS DataBase Reference50-99-7(CAS DataBase Reference)
NIST Chemistry ReferenceGlucose(50-99-7)
EPA Substance Registry SystemDextrose (50-99-7)

Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-63-62-46-36/38-21
Safety Statements 26-36/37-24/25-53-25
WGK Germany 1
RTECS LZ6600000
3
Autoignition Temperature500 °C
TSCA TSCA listed
HS Code 17023051
Storage Class11 - Combustible Solids
Hazardous Substances Data50-99-7(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 25800 mg/kg



Product Application of Dextrose CAS#50-99-7

Glucose is the primary fuel for biological respiration. During digestion, complex sugarsand starches are broken down into glucose (as well as fructose and galactose) in the small intestine.Glucose then moves into the bloodstream and is transported to the liver where glucoseis metabolized through a series of biochemical reactions, collectively referred to as glycolysis.Glycolysis, the breakdown of glucose, occurs in most organisms. In glycolysis, the final productis pyruvate. The fate of pyruvate depends on the type of organism and cellular conditions.In animals, pyruvate is oxidized under aerobic conditions producing carbon dioxide. Underanaerobic conditions in animals, lactate is produced. This occurs in the muscle of humansand other animals. During strenuous conditions the accumulation of lactate causes musclefatigue and soreness. Certain microorganisms, such as yeast, under anaerobic conditions convertpyruvate to carbonic dioxide and ethanol. This is the basis of the production of alcohol.Glycolysis also results in the production of various intermediates used in the synthesis of otherbiomolecules. Depending on the organism, glycolysis takes various forms, with numerousproducts and intermediates possible.

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