N-methyl-D-gluconamide
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
With ammonia borane; palladium/alumina at 78℃; under 975.098 - 48004.8 Torr; for 2h; Temperature; Pressure; Reagent/catalyst; Inert atmosphere; Large scale; | 69.3% |
Conditions | Yield |
---|---|
With hydrogen In water at 10 - 100℃; under 5171.62 - 25858.1 Torr; for 21.5h; | 62.5% |
With nickel kieselguhr; water at 95 - 120℃; under 36775.4 - 102971 Torr; Hydrogenation; | |
With ethanol Hydrierung des Reaktionsprodukts an Palladium-Kohle in Methanol bei 60grad/20-25at; |
Conditions | Yield |
---|---|
With methylamine |
D-glucose
methylamine
A
1-deoxy-1-(methylamino)-D-glucitol
B
N,N`-dimethylethylenediamine
Conditions | Yield |
---|---|
With 5 wt% ruthenium/carbon; hydrogen In water at 124.84℃; under 56255.6 Torr; for 1h; |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In methanol; water | 100% |
2-[1,4,7,10-tetraaza-4,7-di(1-carboxy-2-benzyloxy-ethyl)-10-carboxymethyl-cyclododecane-1-yl]-3-benzyloxypropionic acid
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In water heating to 70°C until a clear soln. was obtained; evapn. (vac.) and isolation after drying to const. weight; elem. anal.; | 100% |
2-[1,4,7,10-tetraaza-4-(1-carboxy-2-benzyloxy-ethyl)-7,10-di(carboxymethyl)-cyclododecane-1-yl]-3-benzyloxypropionic acid
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In water heating to 70°C until a clear soln. was obtained; evapn. (vac.) and isolation after drying to const. weight; elem. anal.; | 100% |
2-[1,4,7,10-tetraaza-4,7,10-tri(carboxymethyl)-cyclododecane-1-yl]-3-benzyloxypropionic acid
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In water heating to 70°C until a clear soln. was obtained; evapn. (vac.) and isolation after drying to const. weight; elem. anal.; | 100% |
2-[1,4,7,10-tetraaza-7-(1-carboxy-2-benzyloxy-ethyl)-4,10-di(carboxymethyl)-cyclododecane-1-yl]-3-benzyloxypropionic acid
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In water heating to 70°C until a clear soln. was obtained; evapn. (vac.) and isolation after drying to const. weight; elem. anal.; | 100% |
D-isoglutamyl-D-tryptophan
1-deoxy-1-(methylamino)-D-glucitol
D-isoglutamyl-D-tryptophan mono-N-methyl-D-glucamine salt
Conditions | Yield |
---|---|
In water at 20℃; pH=~ 7; | 100% |
In water at 20℃; for 168h; pH=Ca. 7; | 100% |
5-chloro-2-([(2-([3-(furan-3-yl)phenyl]amino)-2-oxoehtoxy)acetyl]amino)benzoic acid
1-deoxy-1-(methylamino)-D-glucitol
5-chloro-2-([(2-([3-(furan-3-yl)phenyl]amino)-2-oxoethoxy)acethyl]amino)benzoic acid N-methyl-D-glucaminesalt
Conditions | Yield |
---|---|
In methanol for 0.5h; | 100% |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In methanol at 20℃; for 2h; | 100% |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In water at 20℃; for 1h; | 100% |
Conditions | Yield |
---|---|
In methanol at 20℃; for 72h; | 100% |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In methanol at 20℃; for 0.333333h; | 100% |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; | 100% |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In ethanol for 1h; Reflux; | 100% |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In water at 20℃; Concentration; | 99.5% |
(3β,5β,7α,12α)-3-[[[[[bis[2-[bis(carboxymethyl)amino]ethyl]amino]-acetyl]amino]-acetyl]amino]-7,12-dihydroxycholan-24-oic acid
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In water at 50℃; for 25h; pH=5.0 - 6.8; | 99% |
2,5-dihydroxy-1,4-dithiane-2,5-dicarboxylic acid
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In water at 20℃; for 0.166667h; | 99% |
26-succinate-22-deacetyl-neoboutomellerone
1-deoxy-1-(methylamino)-D-glucitol
26-succinate-22-deacetyl-neoboutomellerone N-methyl-D-glucamine salt
Conditions | Yield |
---|---|
In ethanol; water for 0.166667h; | 99% |
In ethanol; water for 0.166667h; | 99% |
2,5-dioxopyrrolidin-1-yl pent-4-ynoate
1-deoxy-1-(methylamino)-D-glucitol
N-methyl-N-(4-pentynoyl)-D-glucamine
Conditions | Yield |
---|---|
With triethylamine In pyridine; N,N-dimethyl-formamide at 20℃; for 1h; | 99% |
Conditions | Yield |
---|---|
In methanol at 15 - 25℃; for 2h; Solvent; | 99% |
1-deoxy-1-(methylamino)-D-glucitol
3-(triethoxypropyl) isocyanate
Conditions | Yield |
---|---|
In tetrahydrofuran at 80 - 90℃; for 2.5h; | 99% |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In ethanol for 7h; Reflux; | 99% |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In tetrahydrofuran; water at 20℃; for 16h; Solvent; Temperature; | 98.95% |
In isopropyl alcohol at 25 - 50℃; for 1.33333h; Solvent; Sealed tube; | |
In isopropyl alcohol at 25 - 50℃; for 1.33333h; Solvent; Sealed tube; Sonication; |
1-deoxy-1-(methylamino)-D-glucitol
Conditions | Yield |
---|---|
In water at 20℃; Concentration; | 98.9% |
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 20℃; for 0.5h; | 98.7% |
1-deoxy-1-(methylamino)-D-glucitol
4-ethylbenzylaldehyde
(2R,5S)-2-(4-ethylphenyl)-3-methyl-5-(D-arabino-1,2,3,4-tetrahydroxybutyl)oxazolidine
Conditions | Yield |
---|---|
In benzene Heating; | 98% |
1,10-diisocyanatodecane
1-deoxy-1-(methylamino)-D-glucitol
N,N'-decamethylenebis[N''-(1-deoxy-D-glucitol-1-yl)-N''-methylurea]
Conditions | Yield |
---|---|
In 1,4-dioxane; water at 20℃; for 2h; | 98% |
4-(((1S,2S)-2,3-dihydro-1-hydroxy-2-(1H-inden-2-yl)-1H-inden-2-yl)methyl)benzoic acid
1-deoxy-1-(methylamino)-D-glucitol
(2R,3R,4R,5S)-6-(methylamino)hexane-1,2,3,4,5-pentanol 4-(((1S,2S)-1-hydroxy-2,3-dihydro-1H,1'H-[2,2-biinden]-2-yl)methyl)benzoic acid
Conditions | Yield |
---|---|
In methanol at 55℃; | 98% |
In water |
Conditions | Yield |
---|---|
Stage #1: diethylenetriaminopentaacetic acid; 1-deoxy-1-(methylamino)-D-glucitol In water for 0.0333333h; Sonication; Green chemistry; Stage #2: gadolinium(III) oxide In water for 0.3h; Sonication; Green chemistry; | 98% |
Conditions | Yield |
---|---|
Stage #1: aprepitant With dibenzyl [[bis(benzyloxy)phosphoryl]oxy]phosphonate; sodium hexamethyldisilazane In tetrahydrofuran at -3℃; for 2h; Stage #2: 1-deoxy-1-(methylamino)-D-glucitol With palladium 10% on activated carbon; hydrogen In methanol; water for 4h; | 98% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol; water for 4h; | 98% |
N-Methyl-D-Glucamine , with the CAS register number 6284-40-8, is also known as 1-deoxy-1-(methylamino)-d-glucito;1-deoxy-1-(methylamino)hexitol ; glucitol, 1-deoxy-1-(methylamino)-, d- ; meglumin ; methylglucamin ; methylglucamine ; d-glucitol, 1-deoxy-1-(methylamino)- ; d(-)-n-methylglucamine .
The characteristics of this kind of chemical are as below: (1)#H bond acceptors: 6 ; (2)#H bond donors: 6 ; (3)#Freely Rotating Bonds: 11 ; (4)Polar Surface Area: 49.39 ; (5)Index of Refraction: 1.555 ; (6)Molar Refractivity: 45.58 cm3 ; (7)Molar Volume: 141.9 cm3 ; (8)Polarizability: 18.07 ×10-24cm3 ; (9)Surface Tension: 70.8 dyne/cm ; (10)Density: 1.375 g/cm3 ; (11)Flash Point: 251.6 °C ; (12)Enthalpy of Vaporization: 87.2 kJ/mol ; (13)Boiling Point: 490.4 °C at 760 mmHg ; (14)Vapour Pressure: 1.12E-11 mmHg at 25°C .
It is white to almost white crystalline powder. It is soluble in the H2O: 0.1 g/mL(clear, colorless liquid) while in the water 100 g/100 mL (25 ºC). The raw materials are acetaldehyde ammonia and 1-glucose-methylamine schiffbase . Beside, it is sensitive to air and hygroscopic.
Being a kind of irritant chemical, it is harmful to eyes, respiratory system and skin. And while using this chemical, remember to avoid contacting with skin and eyes. If you need more safety information, you could refer to the WGK Germany 3. When it comes to storing method, it should be kept under argon and in a dry place.
N-Methyl-D-Glucamine's product categories are in the below listing of anilines, aromatic amines and nitro compounds, aminosugars, biochemistry, and sugars. As for its uage, it is usualy used as the cosolvent and the surface active agent for contrast agent. We could make it as the following steps:
condense glucose and Monomethylamine and then have the catalytic hydrogenation, finally, you could get this chemical.
In addition, you could obtain the molecular structure by converting the following data information:
SMILES:O[C@H]([C@@H](O)CNC)[C@H](O)[C@H](O)CO
InChI:InChI=1/C7H17NO5/c1-8-2-4(10)6(12)7(13)5(11)3-9/h4-13H,2-3H2,1H3/t4-,5+,6+,7+/m0/s1
InChIKey:MBBZMMPHUWSWHV-BDVNFPICBL
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