![]() Glycogen structure
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Common Name | Glycogen | ||
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CAS Number | 9005-79-2 | Molecular Weight | 666.57800 | |
Density | 1.83g/cm3 | Boiling Point | 1027.2ºC at 760mmHg | |
Molecular Formula | C24H42O21 | Melting Point | 270-280 °C (dec.) | |
MSDS | Chinese USA | Flash Point | 575ºC |
Use of GlycogenGlycogen is a glycolytic intermediates and high-energy phosphates that can serve as a form of energy storage in humans, animals, fungi, and bacteria. |
Name | (2S,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol |
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Synonym | More Synonyms |
Description | Glycogen is a glycolytic intermediates and high-energy phosphates that can serve as a form of energy storage in humans, animals, fungi, and bacteria. |
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Related Catalog | |
Target |
Human Endogenous Metabolite |
References |
Density | 1.83g/cm3 |
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Boiling Point | 1027.2ºC at 760mmHg |
Melting Point | 270-280 °C (dec.) |
Molecular Formula | C24H42O21 |
Molecular Weight | 666.57800 |
Flash Point | 575ºC |
Exact Mass | 666.22200 |
PSA | 347.83000 |
Index of Refraction | 1.687 |
Storage condition | 2-8°C |
Water Solubility | H2O: 20 mg/mL, clear to hazy, faintly yellow |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Risk Phrases | 36/37/38 |
Safety Phrases | S24/25-S26 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | MC2700000 |
Spermidine feeding decreases age-related locomotor activity loss and induces changes in lipid composition.
PLoS ONE 9(7) , e102435, (2014) Spermidine is a natural polyamine involved in many important cellular functions, whose supplementation in food or water increases life span and stress resistance in several model organisms. In this wo... |
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Non-muscle involvement in late-onset glycogenosis II.
Acta Myol. 32(2) , 91-4, (2013) Glycogenosis II (GSD II) is an autosomal recessive lysosomal storage disorder resulting from acid alpha-glucosidase deficiency, subsequent accumulation of glycogen in tissues, impairment of autophagic... |
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Clinical features of Pompe disease.
Acta Myol. 32(2) , 82-4, (2013) Glycogen storage disease type II - also called Pompe disease or acid maltase deficiency - is an autosomal recessive metabolic disorder, caused by an accumulation of glycogen in the lysosome due to def... |
Lyoglycogen |
GLYCOGEN |
Animal starch |
Phytoglycogen |
EINECS 232-683-8 |
Liver starch |
MFCD00081547 |