guanosine hydrate

9-[(4S,2R,3R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-aminohydropurin-6-one

CAS: 118-00-3 C10 H13 N5 O5 MW: 283.24461000

Identification

Nameguanosine hydrate
IUPAC2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one
CAS Number118-00-3
EINECS204-227-8
FDA UNII12133JR80S
Molecular FormulaC10 H13 N5 O5
Molecular Weight283.24461000
MDL NumberMFCD00010182
Nikkaji NumberJ10.076E
Beilstein625911
XlogP3-2.70 (est)

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 239.00 °C. @ 760.00 mm Hg
Flash Point 32.00 °F. TCC ( 0.00 °C. ) (est)
logP (o/w) -2.331 (est)
Soluble in water, 3.153e+004 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesopacifying agents

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral Toxicityintraperitoneal-mouse LD50 500 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements', 'U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#03206']

Safety in Use

Categoryopacifying agents
Recommendation for guanosine hydrate usage levels up tonot for fragrance use.
Recommendation for guanosine hydrate flavor usage levels up tonot for flavor use.

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Potential Uses

biological additives

Natural Occurrence

beet root coffee bean garlic bulb garlic tuber hazelnut pollen wheat petiole

Synonyms

2- amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 2- amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-1,9-dihydro-6H-purin-6-one 2- amino-inosine 2- aminoinosine 9-[(4S,2R,3R,5R)-3,4- dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-aminohydropurin-6-one 9-((2R,3R,4S,5R)-3,4- dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-imino-2,3-dihydro-1H-purin-6(9H)-one 9-((2R,3R,4S,5R)-3,4- dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2-imino-1,2,3,9-tetrahydro-purin-6-one guanine riboside inosine, 2-amino- nucleoside Q vernine PubMed: Wild-type and feedback-resistant phosphoribosyl pyrophosphate synthetases from Bacillus amyloliquefaciens: purification, characterization, and application to increase purine nucleoside production. PubMed: Glutamate: from discovery as a food flavor to role as a basic taste (umami). PubMed: Umami and the foods of classical antiquity. PubMed: Sensory and receptor responses to umami: an overview of pioneering work. PubMed: New developments in umami (enhancing) molecules. PubMed: Sources of umami taste in Cheddar and Swiss cheeses. PubMed: Umami compounds are a determinant of the flavor of potato (Solanum tuberosum L.). PubMed: LC-MS study to reduce ion suppression and to identify N-lactoylguanosine 5'-monophosphate in bonito: a new umami molecule? PubMed: Precursors of chicken flavor. I. Determination of some flavor precursors in chicken muscle. PubMed: Responses to di-sodium guanosine 5'-monophosphate and monosodium L-glutamate in taste receptor cells of rat fungiform papillae. PubMed: Utilization of brewer's yeast cells for the production of food-grade yeast extract. Part 1: Effects of different enzymatic treatments on solid and protein recovery and flavor characteristics. PubMed: Phosphorylation of guanosine using guanosine-inosine kinase from Exiguobacterium acetylicum coupled with ATP regeneration. PubMed: Simultaneous determination of flavor enhancers inosine 5'-monophosphate and guanosine 5'-monophosphate in food preparations by derivative spectrophotometry. PubMed: Parabrachial gustatory neural responses to monosodium glutamate ingested by awake rats. PubMed: Synergistic effects of 5'-nucleotides on rat taste responses to various amino acids. PubMed: Liquid chromatographic determination of flavor enhancers and chloride in food. PubMed: Flavor potentiators.