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DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Favorable price L-Glucose Cas 921-60-8 with top purity Company profile Wuhan Fortuna Chemical Co.,Ltd established in 2006, is a big integrative chemical enterprise being engaged in Pharmaceutical & its intermediates, Food/Feed additives, Fin
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Min.Order:10 Gram
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Type:Trading Company
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Min.Order:1 Gram
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Min.Order:1 Kilogram
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Type:Trading Company
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L-GLUCOSE CAS:921-60-8 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermediates, st
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Min.Order:1 Gram
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Type:Lab/Research institutions
inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
PRODUCT DETAILS
Cas:921-60-8
Min.Order:500 Kilogram
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Min.Order:10 Gram
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inquiryProduct Name:L-GLUCOSESynonyms:L(-)-Glucose,98%;(2S,3R,4S,5S)-2,3,4,5,6-pentahydroxyhexanal;L-Glucose 99%;L(-)-Glucose, 98% 250MG;l-[1,2,3-13C3]glucose;l-[1,2-13C2]glucose;l-[3-13C]glucose;l-[UL-13C6]glucoseCAS:921-60-8MF:C6H12O6MW:180.16EI
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Min.Order:1 Metric Ton
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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Negotiable
Type:Lab/Research institutions
inquiryL-glucose
Conditions | Yield |
---|---|
With DOWEX(α)50WX8-200 In water at 20℃; for 48h; | 100% |
L-glucose
Conditions | Yield |
---|---|
With mercaptoethyl alcohol; Tris*HCl buffer; manganese(ll) chloride; fucose isomerase at 25℃; for 72h; | 28.9% |
Conditions | Yield |
---|---|
With hydrogenchloride In water at 90℃; for 1h; | A 26% B n/a |
Conditions | Yield |
---|---|
With pyridine; hydrogen cyanide Beim Behandeln des Reaktionsprodukts mit wss.Salzsaeure unter gleichzeitigem Hydrieren an Palladium/Bariumsulfat; | |
Multi-step reaction with 2 steps 1: sodium methylate 2: aqueous NaOH-solution / beim anschliessend mit wss.Schwefelsaeure View Scheme |
1-Desoxy-1-nitro-L-gluco-hexitol
L-glucose
Conditions | Yield |
---|---|
With sodium hydroxide beim anschliessend mit wss.Schwefelsaeure; |
L-glucose
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol Yield given; |
L-glucose
Conditions | Yield |
---|---|
With sodium amalgam; sulfuric acid | |
With sodium amalgam; sodium hydrogen oxalate |
Conditions | Yield |
---|---|
das Lacton reagiert; |
Conditions | Yield |
---|---|
Stage #1: L-glucono-1,5-lactone; γ lactone of/the/ l-gluconic acid With sodium tetrahydroborate In water at -5 - 5℃; for 0.333333h; Stage #2: With acetic acid In water |
2-hydroxybenzoyl-β-L-glucopyranosyl (2->1)-β-L-glucopyranosyl (2->1)-β-L-glucopyranosyl (2->1) β-Lglucopyranoside
A
L-glucose
B
salicylic acid
Conditions | Yield |
---|---|
Acidic conditions; |
Conditions | Yield |
---|---|
With trifluoroacetic acid In pyridine at 120℃; for 1h; Inert atmosphere; |
Conditions | Yield |
---|---|
With trifluoroacetic acid In pyridine at 120℃; for 1h; Inert atmosphere; |
Conditions | Yield |
---|---|
With trifluoroacetic acid In pyridine at 120℃; for 1h; Inert atmosphere; |
Conditions | Yield |
---|---|
With trifluoroacetic acid In pyridine at 120℃; for 1h; Inert atmosphere; |
L-glucose
Conditions | Yield |
---|---|
With Dowex In water for 24h; | 14.8 g |
sodium α-d-glucoheptonatehydrate
L-glucose
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: hydrogenchloride / water; methanol / 1 h / Reflux 2: sulfuric acid / water; methanol / 4.25 h / 20 °C 3: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / -40 °C / Reflux 4: SiO2-supported NaIO4 / dichloromethane / 0.5 h 5: Dowex® / water / 24 h View Scheme |
methyl 2,3:4,5:6,7-tri-O-isopropylidene-D-glycero-D-gulo-heptonate
L-glucose
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: sulfuric acid / water; methanol / 4.25 h / 20 °C 2: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / -40 °C / Reflux 3: SiO2-supported NaIO4 / dichloromethane / 0.5 h 4: Dowex® / water / 24 h View Scheme |
methyl 2,3:4,5-di-O-isopropylidene-D-glycero-D-gulo-heptonate
L-glucose
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / -40 °C / Reflux 2: SiO2-supported NaIO4 / dichloromethane / 0.5 h 3: Dowex® / water / 24 h View Scheme |
3-O-β-D-glucopyranosyl-hederagenin 23-O-α-D-ribofuranoside
A
D-ribose
B
L-ribose
C
D-glucose
D
L-glucose
Conditions | Yield |
---|---|
With trifluoroacetic acid In water at 120℃; for 4h; |
A
D-glucose
B
L-glucose
C
5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
Conditions | Yield |
---|---|
With hydrogenchloride; water at 90℃; for 3h; |
L-glucose
Conditions | Yield |
---|---|
With water |
L-glucose
Conditions | Yield |
---|---|
Stage #1: (1R,5R,6R,7R,8S,11S)-11,13-dihydrodehydrocostuslactone-8-O-6’-2’’(E)-butenoyl-β-D-glucopyranoside With hydrogenchloride In methanol; water for 4h; Reflux; Stage #2: With pyridine; L-cysteine methyl ester hydrochloride In methanol; water at 60℃; for 2h; Stage #3: With 2-tolyl isothiocyanate In methanol; water at 60℃; for 1h; |
Conditions | Yield |
---|---|
With hydrogenchloride In water at 105℃; for 4h; |
Conditions | Yield |
---|---|
With water Acidic conditions; |
L-glucose
L-gluconic acid
Conditions | Yield |
---|---|
With 1 wt% Au/TiO2; oxygen In water at 77 - 89℃; under 39547.2 Torr; Flow reactor; | 94% |
With CuO*CeO2 at 180℃; for 4h; Time; Reagent/catalyst; Inert atmosphere; |
L-glucose
2-{5-[5-C-(1,4-anhydro-β-D-erythrotetrofuranosyl)-2-methylfuran-3-yl]-1,3,4-oxadiazol-2-ylthio}acetohydrazide
Conditions | Yield |
---|---|
With acetic acid In ethanol; water Reflux; | 78% |
Conditions | Yield |
---|---|
With oxygen; 1% Au 1% Pt /TiO2 In water at 62℃; under 39547.2 Torr; Temperature; Flow reactor; | A 63% B 15% |
L-glucose
A
L-gluconic acid
B
5-ketogluconic acid
C
ketogulonic acid
Conditions | Yield |
---|---|
With oxygen; 1% Au 1% Pt /TiO2 In water at 80℃; under 39547.2 Torr; Temperature; Flow reactor; | A 14% B 10% C 56% |
L-glucose
N-<4,6-bis(dimethylamino)-1,3,5-triazin-2-yl>trimethylammonium chloride
Conditions | Yield |
---|---|
With potassium hydroxide In water 1.) 0 deg C, 2 h, 2.) 25 deg C, 12 h; | 27% |
pyridine
L-glucose
acetic anhydride
α/β‐L‐glucopyranosyl‐1,2,3,4,5‐pentaacetate
Conditions | Yield |
---|---|
at 0℃; |
Acetyl bromide
L-glucose
2,3,4,6-tetra-O-acetyl-α-L-glucopyranosyl bromide
Conditions | Yield |
---|---|
With acetic acid |
L-glucose
phenylhydrazine acetate
lyxo-[2]Hexosulose-bis-phenylhydrazon
Conditions | Yield |
---|---|
With water phenyl-l-fructosazone; |
L-glucose
O4,O6-((S)-ethylidene)-L-glucose
Conditions | Yield |
---|---|
With sulfuric acid; paracetaldehyde |
L-glucose
1,2:5,6-di-O-isopropylidene-α-L-glucofuranose
Conditions | Yield |
---|---|
With sulfuric acid; copper(II) sulfate; acetone |
L-glucose
sodium acetate
acetic anhydride
α/β‐L‐glucopyranosyl‐1,2,3,4,5‐pentaacetate
L-glucose
1,1-Diphenylhydrazine
glucose-diphenylhydrazone
Conditions | Yield |
---|---|
With ethanol at 100℃; im geschlossenen Rohr; -diphenylhydrazone; |
L-glucose
Amino-acetic acid (3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(5-oxo-2,5-dihydro-furan-3-yl)-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester
Conditions | Yield |
---|---|
With ammonium chloride In ethanol for 4h; Heating; |
L-glucose
L-(-)-α-methylbenzylamine
acetic anhydride
Acetic acid (1S,2S,3S)-2,3,4-triacetoxy-1-{(R)-1-acetoxy-2-[acetyl-(1-phenyl-ethyl)-amino]-ethyl}-butyl ester
Conditions | Yield |
---|---|
With pyridine; sodium cyanoborohydride 1.) methanol-water 2.) 100 deg C, 1 h; Multistep reaction; |
L-glucose
(-)-α-methylbenzylamine
acetic anhydride
Acetic acid (1S,2S,3S)-2,3,4-triacetoxy-1-{(R)-1-acetoxy-2-[acetyl-((S)-1-phenyl-ethyl)-amino]-ethyl}-butyl ester
Conditions | Yield |
---|---|
With pyridine; sodium cyanoborohydride 1.)Methanol, water, room temp. 2.)100 deg C, 1 hour; Multistep reaction; |
Conditions | Yield |
---|---|
With acetic acid In water for 0.5h; Heating; |
Conditions | Yield |
---|---|
complex formation; |
L-glucose
Sucrose
A
leucrose (5-O-α-D-glucopyranosyl-β-D-fructopyranose)
Conditions | Yield |
---|---|
With alternansucrase from Leuconostoc mesenteroides NRRL B-21297 Enzymatic reaction; |
Conditions | Yield |
---|---|
With acetic acid In ethanol at 20 - 75℃; for 3h; Amadori rearrangement; |
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