Appearance:White to off-white powder Storage:Store in tight containers, in a cool dry place Package:25kgs/drum paper-drums and two plastic-bags inside Application:Nucleoside Transportation:Ordinary and safe chemical, suggestion according to IATA DGR
Cas:58-97-9
Min.Order:25 Kilogram
FOB Price: $200.0
Type:Lab/Research institutions
inquiryDayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
Cas:58-97-9
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryTop grade Uridine 5′-monophosphate CAS 58-97-9 with large quantity in stock Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediate
Cas:58-97-9
Min.Order:1 Gram
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Type:Trading Company
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The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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Min.Order:1 Gram
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Type:Manufacturers
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Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
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Min.Order:5 Kiloliter
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Min.Order:1 Kilogram
Negotiable
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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inquiryProduct name Uridine-5'-monophosphate CAS NO. 58-97-9 English name Uridylic Acid Molecular formula C9H13N2O9P Molecular weight 324.1813 Appearance:White powder Storage:Store in c
Appearance:White or off-white powder Storage:Room temperature Package:25kg/drum Application:Used as nucleic acid drug intermediates, health food and biochemical reagents Transportation:Express/Sea/Air Port:Any port in china
Cas:58-97-9
Min.Order:1 Kilogram
Negotiable
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Min.Order:1 Kilogram
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inquiryHanways Chempharm Co., Limited, the former is Hubei Hanways Pharchem CO.,Limited, set up in 2009 in Wuhan, China. We specialize in sourcing and supplying APIs, pharmaceutical intermediates, and fine chemicals for worldwide markets. The founder has d
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inquiryEnglish name Inosine 5’-diphosphate disodium salt(IDP- Na2) English aliases 5’-IDP,2Na; IDP- Na2; 5'- Inosine diphosphatedisodium salt Inosine-5'-diphosphoric acid diso
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Min.Order:10 Gram
Negotiable
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Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At prese
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Min.Order:250 Milligram
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Min.Order:10 Gram
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inquiryHebei Mojin Biotechnology Co., Ltd,Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all em
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inquiryPRODUCT DETAILS
Cas:58-97-9
Min.Order:500 Kilogram
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Type:Lab/Research institutions
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Our advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We have s
95.0%min Appearance:White to off-white powder Storage:2~8℃ Package:packaged according to the needs of customers Application:used for medicine Transportation:by sea by air express Port:china port
Cas:58-97-9
Min.Order:100 Gram
Negotiable
Type:Trading Company
inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
NewCan Biotech Limited was established in 2021 and is primarily engaged in the research, development, production, and sales of sugars, nucleosides, nucleotides, phosphorylated monomers, as well as next-generation antiviral and antitumor drug intermed
Conditions | Yield |
---|---|
With pyridine; benzenesulfonamide for 0.5h; Ambient temperature; | 95% |
Conditions | Yield |
---|---|
Stage #1: uridine With N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; trichlorophosphate at 20℃; for 0.25h; Flow reactor; Green chemistry; Stage #2: With water at 20℃; Temperature; Flow reactor; Green chemistry; chemoselective reaction; | 89% |
With tris(p-nitrophenyl)phosphate at 50℃; Erwina herbicola 47/3 cells; | 78% |
With pyridine; trichlorophosphate |
uridine 5’-monophosphate-imidazole
A
5'-Uridylic Acid
B
[5']uridylic acid monofluoride
Conditions | Yield |
---|---|
With water; lithium fluoride at 25℃; pH=8.6; Reagent/catalyst; pH-value; | A 18.7% B 76.3% |
uridine
A
5'-Uridylic Acid
B
O-((2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl)methyl O,O-dihydrogen phosphorothioate
Conditions | Yield |
---|---|
With trichlorothiophosphine In various solvent(s) for 92h; Ambient temperature; Title compound not separated from byproducts; | A 14.5% B 60.9% |
Conditions | Yield |
---|---|
Stage #1: uridine With N,N,N',N'-tetramethyl-1,8-diaminonaphthalene; trichlorophosphate In dimethyl sulfoxide at 20℃; for 0.25h; Flow reactor; Green chemistry; Stage #2: With water In dimethyl sulfoxide at 20℃; Reagent/catalyst; Flow reactor; Green chemistry; | A 29% B 36% |
triethylamine carbonate
uridine 5'-monophosphate morpholidate
B
5'-Uridylic Acid
Conditions | Yield |
---|---|
Stage #1: fluoromethylenebis(phosphonic acid) tri-n-butylammonium salt With tributyl-amine In ethanol; water at 20℃; for 0.5h; pH=4.5; Stage #2: triethylamine carbonate; uridine 5'-monophosphate morpholidate In dimethyl sulfoxide at 20℃; for 72h; pH=7; Inert atmosphere; | A 20% B n/a |
5'-Uridylic Acid
Conditions | Yield |
---|---|
With isopentyl nitrite In acetone for 24h; | 15% |
Conditions | Yield |
---|---|
With pyridine; trichlorophosphate at -35 - -30℃; anschl. Erwaermen mit wss. H2SO4; | |
With pyrophosphoryl chloride anfangs bei -30grad, und Hydrolysieren des Rktprod. mit Hilfe von LiOH; | |
With pyridine; chlorophosphoric acid dibenzyl ester at -40 - -30℃; anschl. Hydrierung; |
Conditions | Yield |
---|---|
Biosynthese; |
(R)-2',3'-O-benzylideneuridine
5'-Uridylic Acid
Conditions | Yield |
---|---|
With pyridine; chlorophosphoric acid dibenzyl ester at -15℃; anschl. Hydrierung; |
5-phosphoribosyl-1-pyrophosphate
uracil
5'-Uridylic Acid
Conditions | Yield |
---|---|
reversible enzymatische Bildung mit Hilfe von Uracil-phosphoribosyltransferase aus Tumor-Extrakten; | |
reversible enzymatische Bildung mit Hilfe von Uracil-phosphoribosyltransferase aus Lactobacillus-Arten; | |
reversible enzymatische Bildung mit Hilfe von Uracil-phosphoribosyltransferase aus Escherichia coli-Staemmen; | |
With uracil phosphoribosyltransferase from Thermus thermophilus HB8; magnesium chloride In aq. buffer at 60℃; pH=8; Kinetics; Enzymatic reaction; |
5'-Uridylic Acid
Conditions | Yield |
---|---|
With ethanol; platinum Hydrogenation; |
Conditions | Yield |
---|---|
In water at 20℃; Rate constant; Equilibrium constant; pH 8.2-8.8; |
Conditions | Yield |
---|---|
In water at 20℃; Rate constant; pH 8.8; |
uridine 3',5'-cyclic monophosphate
A
uridine-3'-phosphate
B
5'-Uridylic Acid
Conditions | Yield |
---|---|
Lactuca phosphodiesterase In water for 0.416667h; Product distribution; Tris-HCl buffer (pH 6.5); effect of purification stage of phosphodiesterase; |
uridine 3',5'-cyclic monophosphate
A
uridine-3'-phosphate
B
5'-Uridylic Acid
C
uridine 2'-monophosphate
Conditions | Yield |
---|---|
With hydrogenchloride at 90.1℃; Rate constant; |
Phosphoric acid bis-(5-chloro-quinolin-8-yl) ester (2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-hydroxy-4-(tetrahydro-pyran-2-yloxy)-tetrahydro-furan-2-ylmethyl ester
5'-Uridylic Acid
Conditions | Yield |
---|---|
With hydrogenchloride; zinc(II) chloride 1.) pyridine, water, room temp., 24 h, 2.) 22 deg C, 20 h; Yield given. Multistep reaction; |
uridine 5'-(β-D-glucopyranosyl phosphoric acid)
A
D-glucose
B
5'-Uridylic Acid
Conditions | Yield |
---|---|
With hydrogenchloride at 25℃; for 40h; |
O2',O3'-isopropylidene-[5']uridylic acid
5'-Uridylic Acid
Conditions | Yield |
---|---|
With hydrogenchloride at 25℃; for 12h; Yield given; | |
With DOWEX(R) 50WX2-200 |
5'-Uridylic Acid
Conditions | Yield |
---|---|
With hydrogenchloride In water at 20℃; for 2h; |
1-(2,3-O-ethoxymethylidene-β-D-ribofuranosyl)uracil
A
5'-Uridylic Acid
B
uridine
C
O-((2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl)methyl O,O-dihydrogen phosphorothioate
Conditions | Yield |
---|---|
With 1H-imidazole; trichlorophosphate 1.) acetonitrile, room temp. 3 days; 2.) 50percent CH3COOH, 50 deg C, 1 h.; Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; | |
With 1H-imidazole; trichlorophosphate 1.) acetonitrile, room temp. 3 days; 2.) 50percent CH3COOH, 50 deg C, 1 h.; Yield given. Multistep reaction. Title compound not separated from byproducts; |
A
uridine 2',3'-cyclic phosphate
B
uridine-3'-phosphate
C
5'-Uridylic Acid
D
uracil
Conditions | Yield |
---|---|
With sodium persulfate; buffer pH=7 at 70℃; for 4h; Further byproducts given; | A 4 % Chromat. B 25 % Chromat. C 8 % Chromat. D 48 % Chromat. |
A
uridine-3'-phosphate
B
5'-Uridylic Acid
C
uridine 2'-monophosphate
D
uracil
Conditions | Yield |
---|---|
With sodium persulfate; buffer pH=7 at 70℃; for 4h; Further byproducts given; | A 25 % Chromat. B 8 % Chromat. C 43 % Chromat. D 48 % Chromat. |
With sodium persulfate at 70℃; for 4h; Further byproducts given; | A 25 % Chromat. B 8 % Chromat. C 43 % Chromat. D 48 % Chromat. |
A
uridine 2',3'-cyclic phosphate
B
uridine-3'-phosphate
C
5'-Uridylic Acid
D
uridine 2'-monophosphate
E
uracil
Conditions | Yield |
---|---|
With sodium persulfate; sodium phosphate buffer pH=7 In water at 70℃; for 4h; Product distribution; other compounds; | A 1 % Chromat. B 33 % Chromat. C 19 % Chromat. D 2 % Chromat. E 44 % Chromat. |
A
uridine 2',3'-cyclic phosphate
B
uridine-3'-phosphate
C
5'-Uridylic Acid
D
uracil
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; buffer pH=7 at 70℃; for 4h; Further byproducts given; | A 1 % Chromat. B 33 % Chromat. C 19 % Chromat. D 44 % Chromat. |
A
uridine-3'-phosphate
B
5'-Uridylic Acid
C
uridine 2'-monophosphate
D
uracil
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; buffer pH=7 at 70℃; for 4h; Further byproducts given; | A 33 % Chromat. B 19 % Chromat. C 2 % Chromat. D 44 % Chromat. |
A
5'-Uridylic Acid
B
5'-adenosine monophosphate
C
5'-guanosine monophosphate
Conditions | Yield |
---|---|
With SVP (1 unit) In water at 37℃; for 12h; Product distribution; HPLC analysis; no reaction with RNaseT2 or spleen phosphodiesterase; |
Conditions | Yield |
---|---|
With SVP (1 unit) In water at 37℃; for 12h; Product distribution; HPLC analysis; no reaction with RNaseT2 or spleen phosphodiesterase; |
Conditions | Yield |
---|---|
With water at 90.1℃; Rate constant; var. pH; |
Conditions | Yield |
---|---|
With sodium hydroxide at 50℃; for 33h; relative half-life; further hydrolytic conditions: with ribonuclease A, with snake venom phosphodiesterase; further reaction time and temperature; |
5'-Uridylic Acid
1,1'-carbonyldiimidazole
O2',O3'-carbonyl-O5'-(hydroxy-imidazol-1-yl-phosphoryl)-uridine
Conditions | Yield |
---|---|
In acetonitrile for 1h; Milling; | 100% |
Conditions | Yield |
---|---|
Stage #1: 1H-imidazole; 5'-Uridylic Acid With 2,2'-dipyridyldisulphide; triethylamine; triphenylphosphine In dimethyl sulfoxide; N,N-dimethyl-formamide for 3h; Stage #2: With sodium perchlorate; triethylamine In diethyl ether; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone for 2h; | 85% |
Stage #1: 1H-imidazole; 5'-Uridylic Acid With 2,2'-dipyridyldisulphide; triethylamine; triphenylphosphine In dimethyl sulfoxide; N,N-dimethyl-formamide Stage #2: With sodium perchlorate; triethylamine In diethyl ether; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone for 2h; | |
Stage #1: 1H-imidazole; 5'-Uridylic Acid With 2,2'-dipyridyldisulphide; triethylamine; triphenylphosphine In dimethyl sulfoxide; N,N-dimethyl-formamide for 2h; Stage #2: With sodium perchlorate; triethylamine In diethyl ether; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone for 0.5h; |
(1S,2R,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl dihydrogen phosphate
5'-Uridylic Acid
Conditions | Yield |
---|---|
With magnesium chloride hexahydrate; acetylphosphoric acid; acetate kinase; glucose-1-phosphate uridyltransferase; UMP kinase; tris hydrochloride; ATP In water at 37℃; for 5h; Enzymatic reaction; | 84.4% |
5'-Uridylic Acid
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol under 2068.65 Torr; for 24h; | 83% |
Conditions | Yield |
---|---|
With calcium chloride In N,N-dimethyl acetamide Reagent/catalyst; Solvent; | 82% |
5'-Uridylic Acid
Conditions | Yield |
---|---|
Stage #1: diimidazolylpyrophosphate; 5'-Uridylic Acid With calcium chloride In N,N-dimethyl-formamide at 30℃; for 4h; Cooling with ice; Stage #2: With hydrogenchloride; sodium chloride In water Reagent/catalyst; | 80% |
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In water for 6h; pH 5; | 79.1% |
1,2-dioctanoyl-sn-glycero-3-phosphocholine
5'-Uridylic Acid
Conditions | Yield |
---|---|
phospholipase D-P In chloroform at 40℃; for 6h; | 79% |
triethylamine hydrobromide
5'-Uridylic Acid
5-iodouridine-5'-monophosphate triethylammonium
Conditions | Yield |
---|---|
Stage #1: 5'-Uridylic Acid With iodine; nitric acid In chloroform; water at 80℃; for 12h; Stage #2: triethylamine hydrobromide | 77% |
Conditions | Yield |
---|---|
With calcium chloride In dimethyl sulfoxide Reagent/catalyst; Solvent; | 76% |
5'-Uridylic Acid
5-iodouridine-5’-monophosphate
Conditions | Yield |
---|---|
With iodine; nitric acid In chloroform at 90℃; for 18h; | 75% |
With iodine; nitric acid In chloroform at 80℃; for 12h; Product distribution / selectivity; |
5'-Uridylic Acid
cytidine 5'-monophosphate morpholidate
Conditions | Yield |
---|---|
With 4,5-dicyano-1H-imidazole In N,N-dimethyl-formamide at 20℃; for 24h; Reagent/catalyst; Time; Concentration; Temperature; | 68% |
5'-Uridylic Acid
C9H14N2O11P2
Conditions | Yield |
---|---|
With sodium hypophosphate at 60℃; pH 6; | 66% |
5'-Uridylic Acid
2-amino-3,4-di-O-acetyl-2-deoxy-α-D-fucopyranosyl phosphate
Conditions | Yield |
---|---|
Stage #1: 5'-Uridylic Acid With tributyl-amine In 1,4-dioxane for 0.25h; Stage #2: With 1,1'-carbonyldiimidazole In N,N-dimethyl-formamide at 20℃; for 3h; Stage #3: 2-amino-3,4-di-O-acetyl-2-deoxy-α-D-fucopyranosyl phosphate In N,N-dimethyl-formamide at 20℃; for 24h; | 47% |
Conditions | Yield |
---|---|
With lithium chloride In water at 85℃; for 8h; pH=Ca. 2.5; Reagent/catalyst; Inert atmosphere; | 42% |
Conditions | Yield |
---|---|
In 1,4-dioxane for 5h; Ambient temperature; | 38% |
Conditions | Yield |
---|---|
With N-ethylmorpholine buffer; phosphorotriimidazolide at 22℃; for 72h; other 5'-nucleotides, also with phosphorotribenzimidazolide, MnCl2; other time, temperature; | A 25% B 36% |
With phosphorotriimidazolide; magnesium chloride at 22℃; for 72h; N-ethylmorpholine buffer (pH 7.0); | A 25% B 36% |
C18H23N5O5
5'-Uridylic Acid
2-amino-7-(dimethylamidino)mitosene 1-uridylate uridylic acid
Conditions | Yield |
---|---|
In 1,4-dioxane for 16h; Ambient temperature; | 32% |
5'-Uridylic Acid
Conditions | Yield |
---|---|
With tributyl-amine In water; sodium hydrogencarbonate; N,N-dimethyl-formamide | 30% |
Conditions | Yield |
---|---|
Stage #1: 5'-Uridylic Acid; 1,1'-carbonyldiimidazole In N,N-dimethyl-formamide at 20℃; for 3h; Stage #2: α-D-galactofuranosyl bis(triethylammonium)phosphate salt In N,N-dimethyl-formamide at 20℃; for 19h; | 26% |
5'-Uridylic Acid
mitomycin A
2-amino-7-methoxymitosene 1-uridylate uridilic acid salt
Conditions | Yield |
---|---|
In 1,4-dioxane for 3h; Ambient temperature; | 25% |
(1S,2R,3R,4R,5R)-2-acetamido-3,4-dihydroxy-5-hydroxymethyl-cyclohexane-1-phosphate
5'-Uridylic Acid
uridine 5'-(5a-carba-α-D-N-acetylglucosaminopyranosyl diphosphate)
Conditions | Yield |
---|---|
With magnesium chloride hexahydrate; acetylphosphoric acid; acetate kinase; GlcNAc-1-phosphate uridyltransferase; UMP kinase; tris hydrochloride; ATP In water at 37℃; for 5h; Enzymatic reaction; | 23% |
3,4,6-tri-O-acetyl-α-D-glucopyranose-1,2-(t-butylorthoacetat)
5'-Uridylic Acid
uridine 5'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl phosphoric acid)
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 25℃; for 20h; | 21% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 50 - 60℃; | 21% |
5'-Uridylic Acid
C21H22N4O6
2-amino-7-(4-hydroxyanilino)mitosene 1-uridilate uridylic acid salt
Conditions | Yield |
---|---|
In 1,4-dioxane for 3h; Ambient temperature; | 21% |
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