Basic information
- Name:
5'-Inosinic acid
- Superlist Name:
- Inosinic acid
- CAS No.:
131-99-7
- Molecular Structure:
- Formula:
- C10H13N4O8P
- Molecular Weight:
- 348.05
- Deleted CAS:
- 138240-72-9,485-83-6,736074-82-1,801187-33-7
- Synonyms:
- 5'-IMP;IMP;Inosine 5'-(dihydrogen phosphate);Inosine 5'-monophosphate;Inosine5'-phosphate;Inosine-5'-monophosphoric acid;Inosinic acid;
- EINECS:
- 205-045-1
- Density:
- 2.319 g/cm3
- Boiling Point:
- 851.369 °C at 760 mmHg
- Flash Point:
- 468.691 °C
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Chemistry
Product Name: Inosinic acid (131-99-7)
Molecular Formula: C10H13N4O8P
Molecular Weight: 348.206g/mol
Mol File: 131-99-7.mol
Einecs:205-045-1
Storage Temperature: -20°C
Ynonyms of Ethyl Inosinic acid viki (131-99-7) : 5’-inosinicacid ; inosine5’-phosphate ; inosinemonophosphate ; imp ; inosinic acid ; inosine 5'-monophosphate ; inosine-5'-monophosphoric acid ; 1-5'-p .
Uses
Inosinic acid (131-99-7) and its salts such as disodium inosinate are used as flavour enhancers in the food industry,.
Toxicity Data With Reference
| 1. | orl-rat LD50:16 g/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
| 2. | ipr-rat LD50:4850 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
| 3. | scu-rat LD50:3900 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
| 4. | ivn-rat LD50:2730 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
| 5. | orl-mus LD50:12 g/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
| 6. | ipr-mus LD50:5400 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
| 7. | scu-mus LD50:5480 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. | ||
| 8. | ivn-mus LD50:3300 mg/kg | ARTODN Archives of Toxicology. 47 (1981),77. |
Consensus Reports
Reported in EPA TSCA Inventory.
Safety Profile
Moderately toxic by subcutaneous and intravenous routes. When heated to decomposition it emits toxic fumes of POx and NOx.
Specification
Inosinic acid (131-99-7) is a nucleoside monophosphate. Inosinic acid is important in metabolism. It is the ribonucleotide of hypoxanthine and the first nucleotide formed during the synthesis of purine. It is formed by the deamination of adenosine monophosphate, and is hydrolysed to form inosine.Important derivatives of inosinic acid include purine nucleotides found in nucleic acids and adenosine triphosphate, which is used to store chemical energy in muscle and other tissues.