IMP
Synonym(s):I-5′-P;IMP;Inosinic Acid
- CAS NO.:131-99-7
- Empirical Formula: C10H13N4O8P
- Molecular Weight: 348.21
- MDL number: MFCD00066754
- EINECS: 205-045-1
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-01-13 11:13:05
What is IMP?
Chemical properties
White solid
The Uses of IMP
Inosine 5''-monophosphate from Saccharomyces cerevisiae is an IMPDH substrate.
The Uses of IMP
Inosine 5′-monophosphate (IMP) has been used as an umami tastant along with MSG to study their cortical responses and interactions in the human brain. It may be used as a substrate to study the distribution, specificity, and kinetics of inosine-5′-monophosphate dehydrogenase (IMPDH).
What are the applications of Application
Inosine 5′-monophosphate is an IMPDH substrate
Definition
ChEBI: IMP is a purine ribonucleoside 5'-monophosphate having hypoxanthine as the nucleobase. It has a role as a human metabolite, an Escherichia coli metabolite and a mouse metabolite. It is a purine ribonucleoside 5'-monophosphate and an inosine phosphate. It is a conjugate acid of an IMP(2-).
Biochem/physiol Actions
Inosine 5′-monophosphate is a purine nucleotide with a flavor-enhancing property. It acts as a precursor for the synthesis of both guanosine monophosphate (GMP) and adenosine monophosphate (AMP).
Properties of IMP
| Density | 2.31±0.1 g/cm3(Predicted) |
| storage temp. | -20°C |
| solubility | insoluble in EtOH; >70 mg/mL in DMSO; |
| pka | pK1 = 2.4; pK2 = 6.4(at 25℃) |
| form | Solid |
| color | White to off-white |
| Odor | at 100.00?%. odorless |
| Water Solubility | >70 mg/mL in Water |
| CAS DataBase Reference | 131-99-7 |
| EPA Substance Registry System | 5'-Inosinic acid (131-99-7) |
Safety information for IMP
Computed Descriptors for IMP
New Products
Levothyroxine Impurity-F Montelukast EP Impurity-D/Montelukast USP Related Compound C Atorvastatin FXA Impurity/Atorvastatin Cyclic 6-Hydroxy Impurity Sodium Salt Isosulfan blue Keto N-Oxide Impurity Ivermectin Impurity F N-Nitroso des Methyl Tramadol/N-Nitroso-N-Desmethyl-Tramadol DL-beta-(3-Bromophenyl)alanine Tetrabutylammonium perchlorate N,O-Dimethylhydroxylamine hydrochloride (RS)-beta-Amino-beta-(4-bromophenyl)propionic acid 2-Amino-5-bromo-4-(trifluoromethyl)pyridine(RM for Indian lab) N,N CARBONYL DIIMIDAZOLE (R)-BoroLeu-(+)-Pinanediol-CF3COOH 1,4-bis(methylsulfonyl)butane 4-(5-amino-1-methyl-1h-benzoimidazol-2-yl)-butyric acid isopropyl ester. 5-Methyl-1,3-benzenediacetonitrile 4-Fluorothiophenol 1-methyl amino-2,4-dinitro benzene CSA (DL-10-Camphorsulfonic Acid) 2-Hydroxy-4-methylnicotinic acid 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2S)-1-((2S,3S)-3-(2-methylbutyl)-4-oxooxetan-2-yl)pentadecan-2-yl formylleucinate 1-(3,5-dichlorophenyl)-2,2,2-trifluoroethane-1-sulfonyl chloride S-(1-(3,5-dichlorophenyl)-2,2,2-trifluoroethyl) ethanethioateRelated products of tetrahydrofuran








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