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D-ISOSORBIDE

Isosorbide

CAS: 652-67-5

Molecular Formula: C6H10O4

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D-ISOSORBIDE - Names and Identifiers

Name Isosorbide
Synonyms Isosorbide
D-ISOSORBIDE
DIANHYDRO-D-GLUCITOL
DIANHYDRO-D-SORBITOL
Dianhydro-D-glucitol
CAS 652-67-5
EINECS 211-492-3
InChI InChI=1/C6H10O4/c7-3-1-9-6-4(8)2-10-5(3)6/h3-8H,1-2H2/t3-,4-,5+,6+/m1/s1
InChIKey KLDXJTOLSGUMSJ-JGWLITMVSA-N

D-ISOSORBIDE - Physico-chemical Properties

Molecular FormulaC6H10O4
Molar Mass146.14
Density1.0945 (rough estimate)
Melting Point60-63 °C (lit.)
Boling Point175°C/2mmHg(lit.)
Specific Rotation(α)42 º (c=3, H2O)
Flash Point178.8°C
Water SolubilitySoluble in alcohols, water and ketones.
Solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly)
Vapor Presure0.007Pa at 20℃
AppearanceWhite-like to light brown crystals
ColorOff-white to light yellow or beige
Merck14,5224
BRN80510
pKa13.17±0.40(Predicted)
Storage ConditionInert atmosphere,Room Temperature
SensitiveHygroscopic
Refractive Index45 ° (C=5, H2O)
MDLMFCD00064827
UseUsed as a diuretic
In vitro studyIsosorbide increases urine output by increasing the amount of osmotically active solutes in the urine. Osmotic diuretics also increase the osmolality of plasma. Isosorbide is used to prevent or treat chest pain (angina). Its principle of action is to increase the blood and oxygen supply of the heart by relaxing the blood vessels and the heart.
In vivo study Isosorbide (5 mg/kg; a single p.o.) significantly increases the urine volume of rats within 2 hours which lasts through the 8 hour experimental period. Isosorbide (5 mg/kg; a single p.o. 30 min prior to gallium injection) significantly reduces the urinary concentrations of both gallium and calcium in rats. Isosorbide (5 mg/kg; p.o. 30 min prior to gallium injection for 6 d) results in the formation of fewer renal precipitates and histopathologic changes than in the nondiuresed animals.

D-ISOSORBIDE - Risk and Safety

Risk Codes22 - Harmful if swallowed
Safety Description24/25 - Avoid contact with skin and eyes.
WGK Germany2
RTECSLZ4380000
TSCAYes
HS Code29349990

D-ISOSORBIDE - Reference

Reference
Show more
1. Zhu Changliang, Liu Shaoying, Wang Qingyin, Zhang Hua, Wang Gongying. Preparation and properties of poly (butylene carbonate-co-Isosorbide carbonate-co-Spiro carbonate) [J]. Chinese Journal of synthetic chemistry, 2019,27(09):704-711.
2. [IF = 4.598] Xiansong Wang et al."Synthesis and characterization of poly(isosorbide-co-butylene, 5-furandicarboxylate) copolysterers." Eur Polym J. Jun 115:70

D-ISOSORBIDE - Reference Information

LogP-1.39 at 20℃
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
diuretic isosorbide is a sorbitol dehydration derivative, an oral osmotic dehydration diuretic, with a mechanism of action similar to that of Intravenous mannitol and sorbitol. By increasing the plasma osmotic pressure, water in the tissue (including the eye, brain, cerebrospinal fluid, etc.) enters the blood vessels, thereby reducing tissue edema, reducing intraocular pressure, intracranial pressure, and cerebrospinal fluid volume and pressure. Isosorbide is noted for the treatment of cerebral edema and glaucoma.
Application isosorbide as a sorbitol secondary dehydration derivatives, is a new bio-based materials, a wide range of uses of chemical intermediates. Isosorbide has significant medicinal value and is widely used in medicine, food, chemical, feed additives and other industries. The application of isosorbide in Polymer Modification and polymer degradation has begun, further expanding the field of application of isosorbide.
production method isosorbide can be obtained by sorbitol catalytic dehydration, sorbitol can be obtained from starch, sucrose, glucose and other renewable resources are transformed, and have already been large-scale industrial production, mature technology, cheap.
biological activity ISO soramide is a heterocyclic compound derived from glucose and used as a diuretic.
Use used as diuretic
pharmaceutical and chemical intermediates, feed additives
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 21:54:55
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View History
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