Welcome to LookChem.com Sign In|Join Free
  • or

1094-61-7

Post Buying Request

1094-61-7 Suppliers

Recommended suppliersmore

Product FOB Price Min.Order Supply Ability Supplier
beta-nicotinamide mononucleotide
Cas No: 1094-61-7
USD $ 2700.0-3000.0 / Gram 10 Gram 10 Kilogram/Day Kono Chem Co.,Ltd Contact Supplier
β-Nicotinamide Mononucleotide NMN
Cas No: 1094-61-7
No Data 1 Kilogram 1 Metric Ton/Month Xi’an Future Biotechnology Co.,Ltd Contact Supplier
β-NMN CAS NO.1094-61-7 BETA-NICOTINAMIDE MONONUCLEOTIDE
Cas No: 1094-61-7
USD $ 1.0-2.0 / Gram 10 Gram 500 Kilogram/Month Hubei Jusheng Technology Co., Ltd., Contact Supplier
NMN zwitterion Nicotinamide mononucleotide powder cas 1094-61-7
Cas No: 1094-61-7
USD $ 15.0-15.0 / Gram 10 Gram 20 Metric Ton/Month Hebei Yingong New Material Technology Co.,Ltd . Contact Supplier
NMN FACTORY SUPPLY beta NMN powder cas 1094-61-7 BETA-NICOTINAMIDE MONONUCLEOTIDE
Cas No: 1094-61-7
USD $ 1.0-1.0 / Kilogram 1 Kilogram 2000 Kilogram/Year Hebei Guanlang Biotechnology Co., Ltd. Contact Supplier
NMN powder β-Nicotinamide Moonucleotide cas 1094-61-7
Cas No: 1094-61-7
USD $ 350.0-350.0 / Gram 10 Gram 50000 Kilogram/Month HUBEI AOKS BIO-TECH CO.,LTD Contact Supplier
99.3% Beta-Nicotinamide Mononucleotide for Anti-Aging 1094-61-7
Cas No: 1094-61-7
USD $ 4.8-5.0 / Kilogram 1 Kilogram 1000 Kilogram/Year HANWAYS CHEMPHARM CO.,LIMITED Contact Supplier
β-Nicotinamide mononucleotide powder NMN powder CAS:1094-61-7 factory supply high quality
Cas No: 1094-61-7
USD $ 50.0-60.0 / Gram 1 Gram 1000 Metric Ton/Day WUHAN MULEI NEW MATERIAL CO., LTD Contact Supplier
White Powder cas 1094-61-7 β-Nicotinamide mononucleotide
Cas No: 1094-61-7
USD $ 150.0-200.0 / Kilogram 1 Kilogram 50000 Metric Ton/Month Shanlong Biotechnology (hebei) Co., Ltd. Contact Supplier
β-NMN CAS NO.1094-61-7 BETA-NICOTINAMIDE MONONUCLEOTIDE CAS NO.1094-61-7
Cas No: 1094-61-7
No Data 100 Gram 40 Metric Ton/Month Shanghai CRM Import & Export Trading Co., Ltd Contact Supplier

1094-61-7 Usage

Chemical Properties

White Solid

Purification Methods

Purify NMN by passage through a column of Dowex-1 (Cl- form) and washing with H2O until no absorbance is observed at 260 nm. The tubes containing NMN are pooled, adjusted to pH 5.5-6 and evaporated in vacuo to a small volume. This is adjusted to pH 3 with dilute HNO3 in an ice-bath and treated with 20volumes of Me2CO at 0-5o. The heavy white precipitate is collected by centrifugation at 0o. It is best stored wet and frozen or it can be dried to give a gummy residue. It has max 266nm ( 4,600) and min 249nm ( 3600) at pH 7.0 (i.e. no absorption at 340nm). It can be estimated by reaction with CN- or hydrosulfite which form the 4-adducts (equivalent to NADH) which have UV max 340nm ( 6,200). Thus after reaction, an OD340 of one is obtained from a 0.1612mM solution in a 1cm path cuvette. [Plaut & Plaut Biochemical Preparations 5 56 1957, Maplan & Stolzenbach Methods Enzymol 3 899 1957, Kaplan et al. J Am Chem Soc 77 815 1955, Beilstein 22/2 V 168.]

Uses

A product of the extracellular Nicotinamide phosphoribosyltransferase (eNAMPT) reaction and a key NAD+ intermediate. It ameliorates glucose intolerance by restoring NAD+ levels in HFD-induced T2D mice . It also enhances hepatic insulin sensitivity and restores gene expression related to oxidative stress, inflammatory response, and circadian rhythm, partly through SIRT1 activation.
InChI:InChI=1/C11H15N2O8P/c12-10(16)6-2-1-3-13(4-6)11-9(15)8(14)7(21-11)5-20-22(17,18)19/h1-4,7-9,11,14-15H,5H2,(H3-,12,16,17,18,19)/t7-,8-,9-,11-/m1/s1

1094-61-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name NMN zwitterion

1.2 Other means of identification

Product number -
Other names Beta-Nicotinamide Mononucleotide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1094-61-7 SDS

1094-61-7Synthetic route

3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium (β-D-nicotinamide riboside)
23111-00-4

3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium (β-D-nicotinamide riboside)

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With trimethyl phosphite; trichlorophosphate at 0℃; for 12h; Inert atmosphere;88.27%
Stage #1: 3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium (β-D-nicotinamide riboside) With Sodium trimetaphosphate; sodium hydroxide In water at 30℃; for 4h; pH=9;
Stage #2: With hydrogenchloride In water at 10℃; Reagent/catalyst;
68%
With nitromethane; water; trichlorophosphate
3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium bromide
78687-39-5

3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium bromide

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With trimethyl phosphite; trichlorophosphate at -5 - 0℃; for 7h;80%
With trimethyl phosphite; trichlorophosphate at 0℃; for 4h;64%
(3,4-dihydroxy-5-(3-(ethoxycarbonyl)pyridin-1-ium-1-yl)tetrahydrofuran-2-yl)methyl hydrogen phosphate

(3,4-dihydroxy-5-(3-(ethoxycarbonyl)pyridin-1-ium-1-yl)tetrahydrofuran-2-yl)methyl hydrogen phosphate

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With ammonia In acetonitrile at -5 - 5℃; for 1h;80%
nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With ethylenediaminetetraacetic acid; ammonium acetate; zirconium(IV) chloride In ethanol at 50℃; for 0.5h; pH 5;70%
With water; zirconium(IV) chloride at 80℃; for 0.5h; Reagent/catalyst;
C23H24N2O8P(1+)*Cl(1-)

C23H24N2O8P(1+)*Cl(1-)

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With platinum(IV) oxide; hydrogen In deuteromethanol for 12h; Reagent/catalyst;64%
1-(β-D-ribofuranosyl)-nicotinamide
1341-23-7

1-(β-D-ribofuranosyl)-nicotinamide

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With trichlorophosphate In tetrahydrofuran at 0 - 20℃; for 12h;56%
3-carbamoyl-1-(2,4-dinitrophenyl)pyridinium chloride
53406-00-1

3-carbamoyl-1-(2,4-dinitrophenyl)pyridinium chloride

ribose 5-phosphate bis(cyclohexylammonium) salt
87763-86-8

ribose 5-phosphate bis(cyclohexylammonium) salt

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With ammonia 1.) -60 deg C, 36 h; r.t., 1 h; 2.) methanol, ethylene glycol (1:1), 4 deg C, 11 h;35%
nicotinamide
98-92-0

nicotinamide

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

5-phosphoribosyl-1-pyrophosphate

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Enzym aus Erythrocyten;
3-carbamoyl-1-(2,4-dinitrophenyl)pyridinium chloride
53406-00-1

3-carbamoyl-1-(2,4-dinitrophenyl)pyridinium chloride

phosphoribosylamine
14050-66-9

phosphoribosylamine

A

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

B

α-nicotinamide mononucleotide
7298-94-4

α-nicotinamide mononucleotide

C

2,4-Dinitroanilin
97-02-9

2,4-Dinitroanilin

Conditions
ConditionsYield
In methanol at 5℃; for 14h; Yield given;
In methanol at 5℃; for 14h;
β-NAD

β-NAD

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
enzymatische Spaltung;
N1-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-3-aminocarbonylpyridinium bromide
18784-01-5

N1-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-3-aminocarbonylpyridinium bromide

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: NH3 / methanol
2: 80 percent / POCl3, PO(OMe)3 / 7 h / -5 - 0 °C
View Scheme
Multi-step reaction with 2 steps
1: 55 percent / NH3 / methanol / 72 h / -18 °C
2: 64 percent / Phosphoryl chloride, trimethyl phosphate / 4 h / 0 °C
View Scheme
N1-(2,3,5-Tri-O-acetyl-β-D-ribofuranosyl)-3-aminocarbonylpyridinium bromide
78687-38-4

N1-(2,3,5-Tri-O-acetyl-β-D-ribofuranosyl)-3-aminocarbonylpyridinium bromide

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 80 percent / NH3 / methanol / 20 h / -5 - -3 °C
2: 80 percent / POCl3, PO(OMe)3 / 7 h / -5 - 0 °C
View Scheme
adenosine 5'-monophosphate
47287-36-5, 119923-66-9

adenosine 5'-monophosphate

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 91 percent / 1.) H(+), H2O / 1.) 100 deg C, 6 min; 2.) 0 deg C
2: 35 percent / NH3 / 1.) -60 deg C, 36 h; r.t., 1 h; 2.) methanol, ethylene glycol (1:1), 4 deg C, 11 h
View Scheme
1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose
6974-32-9

1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: HBr / CH2Cl2 / 3 h / -20 °C
2: liquid sulphur dioxide
3: 55 percent / NH3 / methanol / 72 h / -18 °C
4: 64 percent / Phosphoryl chloride, trimethyl phosphate / 4 h / 0 °C
View Scheme
Multi-step reaction with 4 steps
1: hydrogen chloride; diethyl ether
2: acetonitrile
3: NH3; methanol
4: POCl3; nitromethane; H2O
View Scheme
2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide
22860-91-9

2,3,5-tri-O-benzoyl-D-ribofuranosyl bromide

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: liquid sulphur dioxide
2: 55 percent / NH3 / methanol / 72 h / -18 °C
3: 64 percent / Phosphoryl chloride, trimethyl phosphate / 4 h / 0 °C
View Scheme
2,3,5-tri-O-acetyl-α-D-ribofuranosyl chloride
105499-44-3

2,3,5-tri-O-acetyl-α-D-ribofuranosyl chloride

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: acetonitrile
2: NH3; methanol
3: POCl3; nitromethane; H2O
View Scheme
nicotinamide
98-92-0

nicotinamide

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: acetonitrile
2: NH3; methanol
3: POCl3; nitromethane; H2O
View Scheme
Multi-step reaction with 3 steps
1: trimethylsilyl trifluoromethanesulfonate / tetrahydrofuran / 12 h / 0 - 20 °C
2: sodium ethanolate / ethanol / 1 h / -5 - 5 °C
3: trichlorophosphate / tetrahydrofuran / 12 h / 0 - 20 °C
View Scheme
Multi-step reaction with 4 steps
1.1: ammonium sulfate / 8 h / 125 °C
2.1: tin(IV) chloride / dichloromethane / 1.5 h / 55 °C
2.2: 0.75 h / 0 °C
3.1: methanol; propylamine / 22 h / -5 °C
4.1: trimethyl phosphite; trichlorophosphate / 12 h / 0 °C / Inert atmosphere
View Scheme
5’,3‘,2’-tri-O-acetyl-1-β-D-ribofuranosylnicotinamide chloride
109527-15-3

5’,3‘,2’-tri-O-acetyl-1-β-D-ribofuranosylnicotinamide chloride

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: NH3; methanol
2: POCl3; nitromethane; H2O
View Scheme
Multi-step reaction with 2 steps
1: hydrogenchloride / methanol / 12 h / Sealed tube
2: trichlorophosphate
View Scheme
3-carbamoyl-1-(tri-O-benzoyl-β-D-ribofuranosyl)-pyridinium; chloride
122620-02-4

3-carbamoyl-1-(tri-O-benzoyl-β-D-ribofuranosyl)-pyridinium; chloride

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: NH3; methanol
2: POCl3; nitromethane; H2O
View Scheme
2,3,5-(tri-O-benzoyl)-D-ribofuranosyl chloride
5991-01-5

2,3,5-(tri-O-benzoyl)-D-ribofuranosyl chloride

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: acetonitrile
2: NH3; methanol
3: POCl3; nitromethane; H2O
View Scheme
3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium trifluoromethanesulfonate

3-carbamoyl-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium trifluoromethanesulfonate

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With trimethyl phosphite; trichlorophosphate at -5 - 0℃; for 12h; Inert atmosphere;
pentasodium 5-phosphoribosyl 1-pyrophosphate

pentasodium 5-phosphoribosyl 1-pyrophosphate

nicotinamide
98-92-0

nicotinamide

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With nicotinamide phosphoribosyltransferase; tris hydrochloride; ATP; magnesium chloride; D,L-dithiothreitol; bovine serum albumin In water at 37℃; Kinetics; Enzymatic reaction;

A

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

B

adenosine 5'-diphosphate
58-64-0

adenosine 5'-diphosphate

C

adenosine
58-61-7

adenosine

Conditions
ConditionsYield
With water; zirconium(IV) oxide at 80℃; for 48h;
[(2R,3R,4R)-3,4-diacetoxy-5-chlorotetrahydrofuran-2-yl]methyl acetate
40554-98-1

[(2R,3R,4R)-3,4-diacetoxy-5-chlorotetrahydrofuran-2-yl]methyl acetate

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: acetonitrile / 0.33 h / 70 °C
2: hydrogenchloride / methanol / 12 h / Sealed tube
3: trichlorophosphate
View Scheme
Multi-step reaction with 3 steps
1: acetonitrile / 50 °C
2: hydrogenchloride / methanol / 12 h / Sealed tube
3: trichlorophosphate
View Scheme
3-carbamoyl-1-((2R,3R,4R,5R)-3,4-diacetoxy-5-(acetoxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium trifluoromethanesulfonate

3-carbamoyl-1-((2R,3R,4R,5R)-3,4-diacetoxy-5-(acetoxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium trifluoromethanesulfonate

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: ammonia / methanol / 24 h / -9 - -8 °C
2: hydrogenchloride / methanol / 8 h / -8 - 0 °C
3: trimethyl phosphite; trichlorophosphate / 24 h / -10 - -7 °C
View Scheme
nicotinamide adenine dinucleotide
76961-04-1

nicotinamide adenine dinucleotide

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With zirconium(IV) chloride In water at 50℃; for 1h;
nicotinamide
98-92-0

nicotinamide

5-phospho-α-D-ribosyl 1-pyrophosphate

5-phospho-α-D-ribosyl 1-pyrophosphate

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
With tris(3-hydroxypropyl)phosphine; nicotinamide phosphoribosyltransferase; tris hydrochloride; ATP; magnesium chloride In water at 37℃; pH=7.5; Kinetics; Reagent/catalyst; Enzymatic reaction;
1,2,3,5-tetraacetylribose
13035-61-5

1,2,3,5-tetraacetylribose

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: trimethylsilyl trifluoromethanesulfonate / tetrahydrofuran / 12 h / 0 - 20 °C
2.1: ammonia / 1 h / -5 - 5 °C
2.2: 1 h / -5 - 5 °C
3.1: trichlorophosphate / tetrahydrofuran / 12 h / 0 - 20 °C
View Scheme
Multi-step reaction with 3 steps
1: trimethylsilyl trifluoromethanesulfonate / tetrahydrofuran / 12 h / 0 - 20 °C
2: sodium ethanolate / ethanol / 1 h / -5 - 5 °C
3: trichlorophosphate / tetrahydrofuran / 12 h / 0 - 20 °C
View Scheme
3-pyridinecarboxylic acid ethyl ester
614-18-6

3-pyridinecarboxylic acid ethyl ester

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: trimethylsilyl trifluoromethanesulfonate / tetrahydrofuran / 12 h / 0 - 20 °C
2.1: ammonia / 1 h / -5 - 5 °C
2.2: 1 h / -5 - 5 °C
3.1: trichlorophosphate / tetrahydrofuran / 12 h / 0 - 20 °C
View Scheme
L-valine
72-18-4

L-valine

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

(S)-1-carboxy-2-methypropan-1-aminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(S)-1-carboxy-2-methypropan-1-aminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water at 10℃; pH=Ca. 3.8 - 4;100%
nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

L-histidine
71-00-1

L-histidine

(S)-1-carboxy-2-(1H-imidazol-4-yl)ethanaminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(S)-1-carboxy-2-(1H-imidazol-4-yl)ethanaminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water at 10℃; pH=Ca. 6 - 6.2;100%
L-threonine
72-19-5

L-threonine

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

(1S,2R)-1-carboxy-2-hydropropan-1-aminium ((2R,3R,4S,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(1S,2R)-1-carboxy-2-hydropropan-1-aminium ((2R,3R,4S,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water at 10℃; pH=Ca. 3.9 - 4.4;100%
nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

L-proline
147-85-3

L-proline

(S)-2-carboxypyrrolidin-1-ium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(S)-2-carboxypyrrolidin-1-ium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water at 10℃; pH=Ca. 3.3 - 3.9;100%
L-lysine
56-87-1

L-lysine

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

(S)-5-amino-5-carboxypentan-1-aminium ((2R,3R,4S,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(S)-5-amino-5-carboxypentan-1-aminium ((2R,3R,4S,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water at 10℃; pH=Ca. 6 - 6.2;100%
L-Aspartic acid
56-84-8

L-Aspartic acid

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

(S)-1,2-dicarboxyethan-1-aminium-((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(S)-1,2-dicarboxyethan-1-aminium-((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water pH=2.99 - 3.39; Inert atmosphere; Cooling with ice;100%
betaine
107-43-7

betaine

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

1-carboxy-N,N,N-trimethylmethanaminium ((2R,35,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

1-carboxy-N,N,N-trimethylmethanaminium ((2R,35,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water at 10℃; for 0.166667h;97%
L-phenylalanine
63-91-2

L-phenylalanine

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

(S)-1-carboxy-2-phenylethan-1-aminium-((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(S)-1-carboxy-2-phenylethan-1-aminium-((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water pH=3.43 - 4; Cooling with ice;96%
L-Cysteine
52-90-4

L-Cysteine

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

(R)-1-carboxy-2-mercaptoethan-1-aminium-((2R,3R,4S,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(R)-1-carboxy-2-mercaptoethan-1-aminium-((2R,3R,4S,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water pH=3.38 - 3.86; Cooling with ice;95%
L-asparagine
70-47-3

L-asparagine

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

(S)-3-amino-1-carboxy-3-oxopropan-1-aminium-((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(S)-3-amino-1-carboxy-3-oxopropan-1-aminium-((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water pH=3.38 - 3.86; Cooling with ice;95%
nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

adenosine 5'-monophosphate
47287-36-5, 119923-66-9

adenosine 5'-monophosphate

nicotinamide adenine dinucleotide
76961-04-1

nicotinamide adenine dinucleotide

Conditions
ConditionsYield
With 1,3-dimercaptopropanol; AdK on PAN gel; NAD pyrophosphorylase; PPiase; potassium acetate; magnesium chloride In water for 3h; Ambient temperature; pH: 7.0;91%
L-methionine
63-68-3

L-methionine

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

(S)-1-carboxy-3-(methylthio)propan-1-aminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(S)-1-carboxy-3-(methylthio)propan-1-aminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water at 10℃; pH=Ca. 4.4 - 4.6;89%
morpholin-4-yl-phosphonic acid mono-5′-[6-(pyrrol-2-yl)-9-β-D-ribofuranosyl-purine]

morpholin-4-yl-phosphonic acid mono-5′-[6-(pyrrol-2-yl)-9-β-D-ribofuranosyl-purine]

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

P1-[6-(pyrrol-2-yl)-purine-9-β-D-ribofuranos-5'-yl]-P2-[nicotinamide-1-β-D-ribofuranos-5′-yl]pyrophosphate

P1-[6-(pyrrol-2-yl)-purine-9-β-D-ribofuranos-5'-yl]-P2-[nicotinamide-1-β-D-ribofuranos-5′-yl]pyrophosphate

Conditions
ConditionsYield
With magnesium sulfate; manganese(ll) chloride In formamide at 20℃; for 12h; Inert atmosphere;87%
nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

glycine
56-40-6

glycine

carboxymethanaminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methvl phosphate

carboxymethanaminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methvl phosphate

Conditions
ConditionsYield
In water pH=3.22 - 3.9; Inert atmosphere; Cooling with ice;85%
L-serin
56-45-1

L-serin

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

(S)-1-carboxy-2-hydroxyethan-1-aminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(S)-1-carboxy-2-hydroxyethan-1-aminium ((2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water pH=3.22 - 3.8; Inert atmosphere; Cooling with ice;83%
((2R,3R,4R,5R)-5-(4-aminothieno[3,4-d]pyrimidin-7-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen triphosphate

((2R,3R,4R,5R)-5-(4-aminothieno[3,4-d]pyrimidin-7-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl dihydrogen triphosphate

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

1-((2R,3R,4R,5R)-5-((((((((2R,3R,4R,5R)-5-(4-aminothieno[3,4-d]pyrimidin-7-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)oxy)(hydroxy)phosphoryl)oxy)methyl)- 3,4-dihydroxytetrahydrofuran-2-yl)-3-carbamoylpyridin-1-ium

1-((2R,3R,4R,5R)-5-((((((((2R,3R,4R,5R)-5-(4-aminothieno[3,4-d]pyrimidin-7-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)oxy)(hydroxy)phosphoryl)oxy)methyl)- 3,4-dihydroxytetrahydrofuran-2-yl)-3-carbamoylpyridin-1-ium

Conditions
ConditionsYield
With Saccharomyces cerevisiae inorganic pyrophosphatase; Homo sapiens recombinant nicotinamide mononucleotide adenylyl transferase 1; potassium chloride; sodium chloride; magnesium chloride In ethanol at 37℃; for 2.16667h; Enzymatic reaction;81%
7-deaza-8-bromoadenosine 5'-monophosphate morpholidate triethylammonium salt

7-deaza-8-bromoadenosine 5'-monophosphate morpholidate triethylammonium salt

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

7-deaza-8-bromo nicotinamide adenine dinucleotide triethylammonium salt
213894-71-4

7-deaza-8-bromo nicotinamide adenine dinucleotide triethylammonium salt

Conditions
ConditionsYield
With magnesium sulfate; formamide; manganese(ll) chloride at 20℃; for 48h;79%
L-alanin
56-41-7

L-alanin

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

C11H15N2O8P*C3H7NO2

C11H15N2O8P*C3H7NO2

Conditions
ConditionsYield
In water pH=3.22-3.8; Inert atmosphere; Cooling with ice;79%
C14H23N6O10P
1278592-46-3

C14H23N6O10P

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

C25H36N8O17P2
1278592-45-2

C25H36N8O17P2

Conditions
ConditionsYield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; magnesium chloride; N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid at 37℃;67%
nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

L-carnitine
541-15-1

L-carnitine

(R)-3-carboxy-2-hydroxy-N,N,N-trimethylpropan-1-aminium ((2R,35,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

(R)-3-carboxy-2-hydroxy-N,N,N-trimethylpropan-1-aminium ((2R,35,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate

Conditions
ConditionsYield
In water at 10℃; for 0.166667h;67%
nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

acetic anhydride
108-24-7

acetic anhydride

2',3'-di-O-acetylnicotinamide mononucleotide
154591-45-4

2',3'-di-O-acetylnicotinamide mononucleotide

Conditions
ConditionsYield
With pyridine In water at 0℃; for 3h;65%
With pyridine In water at 0℃; for 48h;
With pyridine at 0 - 5℃; for 24h; Inert atmosphere;
With pyridine In water at -5 - 0℃; for 24h; Inert atmosphere;
6-N-methyladnenosine 5'-monophosphate morpholidated triethylammonium salt

6-N-methyladnenosine 5'-monophosphate morpholidated triethylammonium salt

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

6-N-methyl nicotinamide adenine dinucleotide triethylammonium salt

6-N-methyl nicotinamide adenine dinucleotide triethylammonium salt

Conditions
ConditionsYield
Stage #1: 6-N-methyladnenosine 5'-monophosphate morpholidated triethylammonium salt; nicotinamide mononucleotide With magnesium sulfate; manganese(ll) chloride In formamide at 20℃; for 48h; Inert atmosphere;
Stage #2: With triethylamine carbonate In formamide; acetonitrile
64%
C26H36N7O9P
1352621-63-6

C26H36N7O9P

nicotinamide mononucleotide
1094-61-7

nicotinamide mononucleotide

8-(3-(Boc-aminomethyl)phenyl) NAD
1352621-54-5

8-(3-(Boc-aminomethyl)phenyl) NAD

Conditions
ConditionsYield
With magnesium sulfate; manganese(ll) chloride In formamide at 20℃; for 24h; Inert atmosphere;61%

Please post your buying leads,so that our qualified suppliers will soon contact you!

*Required Fields