glucurono-1,4-lactone isonicotinoylhydrazone
- CAS No.
- 3691-74-5
- Chemical Name:
- glucurono-1,4-lactone isonicotinoylhydrazone
- Synonyms
- INH-G;Galatone;Glucazide;Mycobactyl;Gluronazide;Glyconiazide;glucurono-1,4-lactone isonicotinoylhydrazone;Glucuronic acid, γ-lactone, 1-[(4-pyridinylcarbonyl)hydrazone]
- CBNumber:
- CB6890728
- Molecular Formula:
- C12H13N3O6
- Molecular Weight:
- 295.24812
- MDL Number:
- MFCD01725299
- MOL File:
- 3691-74-5.mol
| Melting point | -23 °C |
|---|---|
| Boiling point | 436.94°C (rough estimate) |
| Density | 1.3551 (rough estimate) |
| refractive index | 1.5290 (estimate) |
| pka | 11.20±0.46(Predicted) |
| FDA UNII | D71I145DMC |
glucurono-1,4-lactone isonicotinoylhydrazone Chemical Properties,Uses,Production
Originator
Gatalone,Barnes-Hind
Definition
ChEBI: Glyconiazide is an aromatic carboxylic acid and a pyridinemonocarboxylic acid.
Manufacturing Process
2 Methods of producing of d-glucuronolactone isonicotinyl hydrazone:
1. To 88.0 g of D-glucuronolactone, in the bottom of a 3 L round bottom flask,
was added 1.5 liters of methyl alcohol (acetone-free). The mixture was boiled
gently on a steam bath for 10 min, producing a clear solution. To this hot
solution, 70.0 g of isonicotinic acid hydrazide was added all at once. The
mixture was then boiled vigorously for 10 min and the clear solution filtered
without suction through a piece of lens paper into a two liter Erlenmeyer flask.
After the flask had been allowed to stand 24 h at room temperature, crystals
in the form of beautiful white rods and narrow plates were observed. These
crystals were filtered with suction, washed with a small amount of methyl
alcohol, and sucked to complete dryness. The resulting product was dried in a
vacuum desiccator for 3 days. Actual yield was 148.0 g, (yield of better than
99%). On heating the d-glucuronolactone isonicotinyl hydrazone thus formed,
the crystals charred and decomposed with foaming between 150° and 160°C
without any sharp melting point. The new compound was already very pure,
and upon recrystallization from a large amount of methyl or ethyl alcohol
(absolute) showed no appreciable change in physical properties from the
unrecrystallized product.
2. D-Glucuronic acid was liberated from a solution of its sodium salt (12.0 g)
in water (25 ml) by the addition of concentrated hydrochloric acid (5 ml). To
the mixture, sodium acetate (5.0 g) was added to remove the excess of the
mineral acid. Isonicotinic acid hydrazide (7.0 g) was then introduced into the
clear solution and mixing accomplished by thorough shaking. Methyl alcohol
(250 ml) was added and the mixture boiled on a steam bath for 10 min. A
white crystalline precipitate started to separate from the solution after a few
minutes heating and was allowed to stand overnight at room temperature
before filtering. The crystals (white small rods) were sucked to dryness,
washed with a small amount of absolute methanol and again sucked to
dryness. The product was further dried in a vacuum desiccator for 24 h. Yield:
25-50%. The hydrazone melted at 150°-160°C (dec.).
Therapeutic Function
Antitubercular
glucurono-1,4-lactone isonicotinoylhydrazone Preparation Products And Raw materials
glucurono-1,4-lactone isonicotinoylhydrazone Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| CHEMICAL LAND21 | -- | sales21@chemicalland21.com | South Korea | 6315 | 74 |
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| CHEMICAL LAND21 | 74 |