Size | Price | Stock | Qty |
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5g |
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Other Sizes |
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ln Vitro |
The lactone (cyclic ester) of D-gluconic acid is called D-(+)-Glucono-1,5-lactone. Common sources of D-(+)-Glucono-1,5-lactone include wine, fruit juices, honey, and personal lubricants. Though it is only approximately one-third as acidic as citric acid, D-(+)-glucono-1,5-lactone is neutral but hydrolyzes in water to the acidic gluconic acid, which gives food a rich flavor. One gram of D-(+)-glucono-1,5-lactone yields about the same metabolic energy as one gram of sugar after being converted to glucose. GDL hydrolyzes to gluconic acid when added to water, creating a chemical equilibrium between the lactone and acid forms. The rate of hydrolysis of D-(+)-Glucono-1,5-lactone is accelerated by heating and high pH [1].
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Toxicity/Toxicokinetics |
Non-Human Toxicity Values
LD50 Rabbit 7630 mg/kg /Sodium Gluconate/ |
References | |
Additional Infomation |
D-glucono-1,5-lactone is an aldono-1,5-lactone obtained from D-gluconic acid. It has a role as an animal metabolite and a mouse metabolite. It is a gluconolactone and an aldono-1,5-lactone. It is functionally related to a D-gluconic acid.
Gluconolactone is a naturally-occurring food additive used as a sequestrant, an acidifier, or a curing, pickling, or leavening agent. It is a cyclic ester of D-gluconic acid. Pure gluconolactone is a white odorless crystalline powder. Gluconolactone is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Gluconolactone is a Calculi Dissolution Agent. The mechanism of action of gluconolactone is as an Irrigation. Gluconolactone has been reported in Tetranychus urticae, Lotus burttii, and other organisms with data available. Gluconolactone is a naturally occurring polyhydroxy acid (PHA) with metal chelating, moisturizing and antioxidant activity. Gluconolactone can be produced by enzymatic oxidation of D-glucose oxidation. Its ability in free radicals scavenging accounts for its antioxidant property. It is used in cosmetic product and as a coagulant in tofu processing. (NCI05) Therapeutic Uses MEDICATION (VET): ...Mixture in urine helps dissolve urinary tract stones containing calcium carbonate, tricalcium phosphate, calcium oxalates, & magnesium ammonium phosphates but usually none containing uric acid, urates, cystineine, or some oxalates. MEDICATION (VET): 0.5% Solution can be used for irrigating the urethra & bladder when indicated. Similar strength as a rinse can help maintain in dwelling urethral catheters free of calcification. |
Molecular Formula |
C6H10O6
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Molecular Weight |
178.1400
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Exact Mass |
178.047
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CAS # |
90-80-2
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Related CAS # |
D-(+)-Glucono-1,5-lactone-1-13C
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PubChem CID |
7027
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Appearance |
White to off-white solid powder
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Density |
0.6
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Boiling Point |
230.35°C
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Melting Point |
151-155 ºC
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Flash Point |
192.3±20.3 °C
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Vapour Pressure |
0.0±2.4 mmHg at 25°C
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Index of Refraction |
1.608
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LogP |
-2.38
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Hydrogen Bond Donor Count |
4
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Hydrogen Bond Acceptor Count |
6
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Rotatable Bond Count |
1
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Heavy Atom Count |
12
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Complexity |
181
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Defined Atom Stereocenter Count |
4
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SMILES |
C([C@@H]1[C@H]([C@@H]([C@H](C(=O)O1)O)O)O)O
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InChi Key |
PHOQVHQSTUBQQK-SQOUGZDYSA-N
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InChi Code |
InChI=1S/C6H10O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-5,7-10H,1H2/t2-,3-,4+,5-/m1/s1
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Chemical Name |
(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-one
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HS Tariff Code |
2934.99.9001
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Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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Solubility (In Vitro) |
H2O : ≥ 100 mg/mL (~561.36 mM)
DMSO : ~100 mg/mL (~561.36 mM) |
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Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.5 mg/mL (14.03 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 2: ≥ 2.5 mg/mL (14.03 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution. View More
Solubility in Formulation 3: 150 mg/mL (842.03 mM) in PBS (add these co-solvents sequentially from left to right, and one by one), clear solution; with ultrasonication. |
Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
1 mM | 5.6136 mL | 28.0678 mL | 56.1356 mL | |
5 mM | 1.1227 mL | 5.6136 mL | 11.2271 mL | |
10 mM | 0.5614 mL | 2.8068 mL | 5.6136 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration: mg/mL;
Method for preparing DMSO stock solution: mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation::Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O,mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.