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Cas Database

Name	INOSINIC ACID	EINECS	205-045-1
CAS No.	131-99-7	Density	2.319 g/cm³
PSA	189.83000	LogP	-2.15190
Solubility	N/A	Melting Point	N/A
Formula	C₁₀H₁₃N₄O₈P	Boiling Point	851.369 °C at 760 mmHg
Molecular Weight	348.209	Flash Point	468.691 °C
Transport Information	N/A	Appearance	N/A
Safety	22-24/25	Risk Codes	N/A
Molecular Structure		Hazard Symbols	N/A
Synonyms	5'-IMP;IMP;Inosine 5'-(dihydrogen phosphate);Inosine 5'-monophosphate;Inosine5'-phosphate;Inosine-5'-monophosphoric acid;Inosinic acid;	Article Data	54

INOSINIC ACID Synthetic route

: 78681-84-2
Phosphoric acid (3aR,4R,6R,6aR)-2,2-dimethyl-6-(6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester bis-(2,2,2-tribromo-ethyl) ester

: 131-99-7
5'-inosine monophosphate

Conditions

Conditions	Yield
With Nafion 125; lithium perchlorate In N,N-dimethyl-formamide; acetonitrile electrolysis;	89%

: 61-19-8
5'-adenosine monophosphate

A: 131-99-7
5'-inosine monophosphate

B: 58-64-0
adenosine 5'-diphosphate

C: 56-65-5
ATP

Conditions

Conditions	Yield
With zinc(II) chloride In methanol at 25℃; Product distribution; biosynthesis; various typ-, and conc. of reagent;
In methanol at 25℃; biosynthesis by Candida boidnii No. 2201; pH = 6.5;	A 14.8 mmol B 36.8 mmol C 24.0 mmol
With zinc(II) chloride In methanol at 25℃; biosynthesis by Candida boidnii No. 2201; pH = 6.5;	A 2.0 mmol B n/a C 36.8 mmol
In methanol at 25℃; biosynthesis by Candida boidnii No. 2201; pH = 6.5;	A 14.8 mmol B 1.1 mmol C 24.0 mmol

: 58-63-9
Inosine

: 131-99-7
5'-inosine monophosphate

Conditions

Conditions	Yield
With triethyl phosphate; trichlorophosphate In water at 0℃; for 2h; Rate constant; Product distribution; var. reaction conditions;	91 % Chromat.
With potassium dihydrogenphosphate; D-glucose; guanosine-inosine kinase from Exiguobacterium acetylicum In various solvent(s) at 32℃; pH=7.2; Enzymatic reaction;
With DL-dithiothreitol; recombinant cytosolic 5'-nucleotidase II; ATP In various solvent(s) at 37℃; pH=7.4; Enzyme kinetics; Further Variations:; Reagents;
With sodium pyrophosphate; sodium acetate buffer; Escherichia blattae wild type phosphotransferase at 30℃; pH=5.0; Enzyme kinetics; Further Variations:; Reagents;
With trimethyl phosphite; trichlorophosphate at 0℃;

: 97-55-2, 7540-64-9, 99945-37-6, 130384-52-0
5-phosphoribosyl-1-pyrophosphate

: 68-94-0
hypoxanthine

: 131-99-7
5'-inosine monophosphate

Conditions

Conditions	Yield
With Toxoplasma gondii phosphoribosyltransferase In alkaline aq. solution at 37℃; pH=7.4; Enzyme kinetics;

: 58-63-9
Inosine

A: 572-47-4
3'-inosine monophosphate

B: 131-99-7
5'-inosine monophosphate

Conditions

Conditions	Yield
With disodium pyrophoshate; Shigella flexneri acid phosphatase In various solvent(s) at 30℃; pH=5.0; Enzyme kinetics; Further Variations:; Reagents;

: 68-94-0
hypoxanthine

: 5-phospho-α-D-ribosyl 1-pyrophosphate

: 131-99-7
5'-inosine monophosphate

Conditions

Conditions	Yield
With hypoxanthine phosphoribosyltransferase Enzyme kinetics; Further Variations:; Reagents;

: 4229-50-9
N6-methyl AMP

: 131-99-7
5'-inosine monophosphate

Conditions

Conditions	Yield
With diothiothreitol; water at 37℃; pH=6.8; Enzyme kinetics;

5'-CTCCTTCCATACGGTGCACCTTCCTC-3': 5'-CTCCTTCCATACGGTGCACCTTCCTC-3'

5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-CATGTACCGATAAGCGTATTATGGAAGGAGGCGTTATGAGGGGTCCA-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/bis(adenosine 5'-monophosphate) complex: 5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-CATGTACCGATAAGCGTATTATGGAAGGAGGCGTTATGAGGGGTCCA-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/bis(adenosine 5'-monophosphate) complex

A 5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-CATGTACCGATAAGCGTATTATGGAAGGAGGCGTTATGAGGGGTCCA-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/5'-CTCCTTCCATACGGTGCACCTTCCTC-3': 5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-CATGTACCGATAAGCGTATTATGGAAGGAGGCGTTATGAGGGGTCCA-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/5'-CTCCTTCCATACGGTGCACCTTCCTC-3'

B: 131-99-7
5'-inosine monophosphate

Conditions

Conditions	Yield
With 4-(2-hydroxyethyl)piperazine-1-ethanesulfonic acid sodium salt; sodium chloride; adenosine deaminase In water at 25 - 70℃; for 1.33333h; pH=7.4; Enzymatic reaction;

5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-AGGTGCACGTGGTCCAGTGCTGCAGTG-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/adenosine 5'-monophosphate complex: 5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-AGGTGCACGTGGTCCAGTGCTGCAGTG-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/adenosine 5'-monophosphate complex

A 5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-AGGTGCACGTGGTCCAGTGCTGCAGTG-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/5'-CTCCTTCCATACGGTGCACCTTCCTC-3': 5'-Cy5-ATACGCTTATCGGTACATGAGCACTGCAGCACTGGACCAC-Iowa black RQ-3'/5'-AGGTGCACGTGGTCCAGTGCTGCAGTG-3'/5'-ACCTGGGGGAGTATTGCGGAGGAAGGTGCGTGGTCCAGTGCTGCAGTG-3'/5'-CTCCTTCCATACGGTGCACCTTCCTC-3'

B: 131-99-7
5'-inosine monophosphate

Conditions

Conditions	Yield
With adenosine deaminase aq. buffer; Enzymatic reaction;

: C24H24N6O9PPol

: 131-99-7
5'-inosine monophosphate

Conditions

Conditions	Yield
Stage #1: C24H24N6O9PPol With ammonium hydroxide In water at 55℃; for 15h; solid phase reaction; Stage #2: With trifluoroacetic acid In dichloromethane at 20℃; for 0.333333h; solid phase reaction;

INOSINIC ACID Chemical Properties

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 .

INOSINIC ACID Uses

Inosinic acid (131-99-7) and its salts such as disodium inosinate are used as flavour enhancers in the food industry,.

INOSINIC ACID 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.

INOSINIC ACID Consensus Reports

Reported in EPA TSCA Inventory.

INOSINIC ACID Safety Profile

Moderately toxic by subcutaneous and intravenous routes. When heated to decomposition it emits toxic fumes of PO_x and NO_x.

INOSINIC ACID 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.

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