Inosine 5'-Monophosphate Disodium Salt Hydrate - 10mM in Water , CAS No.4691-65-0

CAS: 4691-65-0 Cat. No.: I424099 Peso molecular: 392.17 Beilstein Registry Number: 31,26 Número EC: 225-146-4 PubChem CID: 135414245
Disponible para pedir
GRADE & PURITY 10mM in Water
Synonyms
Disodium 5'-inosinate|4691-65-0|Disodium inosinate|Sodium inosinate|5'-Imp disodium salt|IMP disodium salt|5'-INOSINIC ACID, DISODIUM SALT|FEMA No. 3669|Inosine 5'-monophosphate disodium salt|Disodium inosine-5'-monophosphate|Inosine 5'-monophosphate diso
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
I424099-1ml
2

47,90US$

69,90US$
Guardar 22,00 US$ (31.47%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

10mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Inosine 5′-monophosphate (IMP) is used as a substrate to study the distribution, specificity and kinetics of inosine-5′-monophosphate dehydrogenase (IMPDH).

Specifications

Sinónimos
Disodium 5'-inosinate | 4691-65-0 | Disodium inosinate | Sodium inosinate | 5'-Imp disodium salt | IMP disodium salt | 5'-INOSINIC ACID, DISODIUM SALT | FEMA No. 3669 | Inosine 5'-monophosphate disodium salt | Disodium inosine-5'-monophosphate | Inosine 5'-monophosphate diso
Especificaciones y pureza
10mM in Water
Mecanismos bioquímicos y fisiológicos
Inosine monophosphate, or inosinic acid, is the ribonucleotide of hypoxanthine and the first nucleotide formed during purine synthesis.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicasC1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)COP(=O)([O-])[O-])O)O.[Na+].[Na+]
IUPAC Namedisodium;[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methyl phosphate
InChIKeyAANLCWYVVNBGEE-IDIVVRGQSA-L
INCHI1S/C10H13N4O8P.2Na/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17;;/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20);;/q;2*+1/p-2/t4-,6-,7-,10-;;/m1../s1
Isómeros SMILES C1=NC2=C(C(=O)N1)N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)([O-])[O-])O)O.[Na+].[Na+]
RTECS NM7519500
CAS alternativo 352195-40-5
PubChem CID 135414245
Peso molecular 392.17
Beilstein 31,26
Reaxy-Rn 5722042

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
ClasePurine nucleotides
SubclassPurine ribonucleotides
Intermediate Tree Nodes Not available
Direct ParentPurine ribonucleoside monophosphates
Alternative Parents Pentose phosphates  Glycosylamines  6-oxopurines  Hypoxanthines  Monosaccharide phosphates  Pyrimidones  Alkyl phosphates  N-substituted imidazoles  Vinylogous amides  Tetrahydrofurans  Heteroaromatic compounds  Secondary alcohols  1,2-diols  Oxacyclic compounds  Azacyclic compounds  Organic sodium salts  Organic zwitterions  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  Organic oxides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Pyrimidone - N-substituted imidazole - Organic phosphoric acid derivative - Monosaccharide - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Heteroaromatic compound - Imidazole - Tetrahydrofuran - Azole - Vinylogous amide - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Organic alkali metal salt - Organic salt - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic zwitterion - Alcohol - Organic sodium salt - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Peso molecular392.170 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count10
Rotatable Bond Count3
Exact Mass392.011 Da
Monoisotopic Mass392.011 Da
Topological Polar Surface Area181.000 Ų
Heavy Atom Count25
Formal Charge0
Complexity543.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Tiantian Tang, Min Zhang, Yaping Liu.  (2023)  Valorization of meat and bone residue by ultrasound and high voltage electrostatic field assisted two-stage enzymatic hydrolysis: Nutritional characteristics and flavor analysis.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2023.103203]
2. Ting Zou, You Han, Xinxue Li, Wei Li, Jinli Zhang, Yan Fu.  (2018)  Unexpected catalytic activity of Pd(II)-coordinated nucleotides in hydrogenation reduction.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2018.10.034]
3. Lijun Tan, Shasha Zheng, Yong Xie, Wendi Zhang, Baocai Xu.  (2025)  Sustained photodynamic H2O2 generation via disodium 5′-inosinate enhances cooked meat preservation by membrane-targeted antibacterial action.  Innovative Food Science & Emerging Technologies,      [PMID:] [10.1016/j.ifset.2025.104150]
4. Yuwei Liu, Yuting Wang, Ziyi Liu, Chang Li, Qiang Yu, Jianhua Xie, You Long, Qianzhu E, Yi Chen.  (2025)  Flavor modulation of braised He Bao carp (Cyprinus carpio) by natural plant spices: Insights from GC–MS, GC–IMS, E-nose, E-tongue, and molecular docking analyses.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2025.108101]
5. Xingyue Chen, Jiachen Lu, Zhaojun Wu, Haopeng Zhang, Wei Zheng, Huanghe Zeng, Dongbiao Chang, Jie Weng, Jinsheng Li, Tailin Guo.  (2026)  Infection protection, immune regulation and epithelial regeneration trifunctional hydrogel for treatment of burn wounds.  Materials Today Bio,      [PMID:41585437] [10.1016/j.mtbio.2026.102788]
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.