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L-Glutamic acid Factory L(+)-Glutamic acid CAS 56-86-0 2-Aminoglutaric acid Glutamic acid L-Glutamic acid Manufacturer High quality Best price In stock factory CAS 56-86-0 L-Glutamic acid COA TDS price MSDS highly quality and immedaite
Cas:56-86-0
Min.Order:5 Kiloliter
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Type:Manufacturers
inquiryProduct Description Product Name: L-Glutamic acid Synonyms: L-GLUTAMIC ACID extrapure;(S)-2-Aminopentanedioic acid, Acidum glutamicum, Glu;(S)-2-Aminopentanedioic acid, Glu;L-GLUTAMIC ACIDRESEARCH GRADE;L-Glutanmic;L-Glu
Cas:56-86-0
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inquiryProduct name: L-Glutamic Acid CAS No.:56-86-0 Molecule Formula:C5H9NO4 Molecule Weight:147.13 Purity: 99.5% Package: 25kg/drum Description:White crystalline powder Manufacturer standard: FCCIV, AJI, USP, EP. Items
Cas:56-86-0
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Items Standard Result Assay 98%min ----------------------------------------------------------------------------------------------
Cas:56-86-0
Min.Order:1 Gram
FOB Price: $100.0 / 500.0
Type:Manufacturers
inquiryProduct Name: L-Glutamic acid Synonyms: FEMA 3285;GLU;GLUTAMIC ACID, L-;GLUTAMIC ACID BASE;GLUTACID;H-L-GLU-OH;H-GLU-OH;L-ALPHA-AMINOGLUTARIC ACID C… Founded in 2014, as a professional international pharmaceutical corporation, headquartere
Product description: Product name L-Glutamic acid CAS number 56-86-0 Assay ≥99% Appearance White crystalline powder Capacity 20mt/year Application Food additives Mor
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Min.Order:10 Gram
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Type:Lab/Research institutions
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Min.Order:1 Gram
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inquiryUnique advantages for L-Glutamic acid Cas 56-86-0 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White crystals or crystalline powder Storage:Store at RT Package:25kg/
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Min.Order:100 Kilogram
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Type:Trading Company
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Cas:56-86-0
Min.Order:0 Metric Ton
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Type:Trading Company
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Min.Order:25 Kilogram
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Type:Manufacturers
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Min.Order:1 Gram
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Type:Manufacturers
inquiryADVANTAGE: 1. More than 3,000 Chinese medicine reference substances / standard products available from stock, issued on the same day, multiple cities can be delivered the next day 2. The products are provided with COA, HPLC, NMR, quality assurance,
Zorui combines R&D, production and sales into its operations, While continuously providing high-quality raw materials, we also provide and optimize technical solutions for customers to achieve mutual benefit. We adhere to the "quality, integ
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Min.Order:10 Gram
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Type:Trading Company
inquiryOur 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
Name: L-Glutamic acid Synonyms: L-Glutamic acid (S)-2-Aminopentanedioic acid CAS:56-86-0 MF: C5H9NO4 Appearance:White powder Storage:Store in cool and dry place, away from sun light. Package:25kg/drum Application:Food Additives Transportation:B
Appearance:White crystalline powder Storage:ln stock Package:25kg/Barrel Application:Used in pharmaceuticals, food additives, nutrition fortifiers Transportation:Express/Sea/Air Port:Any port in China
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Min.Order:1 Metric Ton
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Type:Lab/Research institutions
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Cas:56-86-0
Min.Order:10 Gram
Negotiable
Type:Other
inquiryHanways chempharm is a specialized company concentrating on the R&D, production, marketing and technical service of APIs and pharmaceutical intermediates. The marketing department is located in Wuhan. We have two GMP facilities in Hubei Pr
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:56-86-0
Min.Order:10 Gram
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Type:Trading Company
inquiryProduct Name: L-Glutamic acid CAS: 56-86-0 MF: C5H9NO4 MW: 147.13 EINECS: 200-293-7 Mol File: 56-86-0.mol L-Glutamic acid Structure L-Glutamic acid Chemical Properties Melting point 205 °C (dec.) (lit.) alpha 32 º
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L-Glutamic acid CAS: 56-86-0 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 intermediat
Cas:56-86-0
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryL-glutamic acid
Conditions | Yield |
---|---|
With dimethylsulfide; hydrogen fluoride; methoxybenzene at 0℃; for 1h; Product distribution; Rate constant; other concentration of reagents; | 100% |
With dimethylsulfide; trifluorormethanesulfonic acid; 30 (v/v); trifluoroacetic acid at 0℃; for 4h; Yield given; | |
With trifluoroacetic acid In dichloromethane at 20℃; Rate constant; | |
With recombinant Pseudomonas nitroreducens IFO12694 γ-glutamyltranspeptidase at 30℃; for 0.0333333h; pH=10.5; aq. buffer; Enzymatic reaction; | |
With E. coli BL21 Star (DE3) S30 extract In aq. buffer at 37℃; for 6h; pH=7.5; |
Boc-Glu(OBzl)-OH
L-glutamic acid
Conditions | Yield |
---|---|
With Nafion H; dimethylsulfide; 3-methyl-phenol; trifluoroacetic acid for 3h; | 100% |
With dimethylsulfide; hydrogen fluoride at 0℃; for 2h; Product distribution; Var.: HF in anisole; | 100% |
Z(OMe)-Glu(OBzl)-OH
L-glutamic acid
Conditions | Yield |
---|---|
With trimethylsilyl trifluoromethanesulfonate; diphenyl sulfide In trifluoroacetic acid at 0℃; for 0.5h; Product distribution; New peptide deprotection procedure: hard-soft acid-base concept; the role of soft bases (thioanisole, dimethylsulfide, diphenylsulfide) employed.; | 100% |
N-α-tert-butyloxycarbonyl-glutamic acid, γ-cyclohexyl ester
L-glutamic acid
Conditions | Yield |
---|---|
With phenylthiotrimethylsilane; pertrimethylsilylated Nafion; 3-methyl-phenol; trifluoroacetic acid for 3h; | 100% |
N-allyloxycarbonyl α-allyl-L-glutamate
L-glutamic acid
Conditions | Yield |
---|---|
With diethylamine; tetrakis(triphenylphosphine) palladium(0) In dichloromethane at 20℃; for 3h; deallylation; | 100% |
Conditions | Yield |
---|---|
With hydrogen In ethanol for 1.33333h; | 98% |
With hydrogen; hydroxyapatite-bound Pd In methanol at 40℃; for 12h; | 96% |
With hydrogen In ethanol at 20℃; under 760.051 Torr; for 3h; | 95% |
(S)-(N-benzyl-N-benzyloxycarbonyl)glutamic acid
L-glutamic acid
Conditions | Yield |
---|---|
With hydrogen; palladium dihydroxide In water; acetic acid for 45h; Ambient temperature; | 97% |
Boc-Glu(OtBu)-OH
L-glutamic acid
Conditions | Yield |
---|---|
With triethylsilane; trifluoroacetic acid In dichloromethane for 1.08333h; Ambient temperature; | 96% |
Conditions | Yield |
---|---|
With tetradecyl(trihexyl)phosphonium bistriflamide; trifluoroacetic acid at 130℃; for 0.166667h; Ionic liquid; | 96% |
Conditions | Yield |
---|---|
With sodium hydroxide; zinc(II) sulfate In water at 105℃; for 50h; Product distribution; Mechanism; Heating; at pH 6.5; variation of amount of substrate and added salts, reaction time and temperature; further metal salts; | 93.1% |
Rate constant; | |
Multi-step reaction with 7 steps 1.1: 100 percent / 1,3-dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / CH2Cl2 / 0 - 20 °C 2.1: 100 percent / 3-chloroperoxybenzoic acid / CH2Cl2 / 4 h / 0 °C 3.1: bis(cyclopentadienyl)zirconium dichloride; silver(I) perchlorate / CH2Cl2 / 48 h 4.1: 9.40 g / 4-(dimethylamino)pyridine / acetonitrile / 1.5 h / 20 °C 5.1: sodium bis(trimethylsilyl)amide; N,N'-dimethylpropyleneurea / tetrahydrofuran / 0.5 h / -78 °C 5.2: tetrahydrofuran / 2 h 6.1: 6.48 g / hydrogen peroxide / tetrahydrofuran / 2 h / 20 °C 7.1: hydrogen / palladium on carbon / methanol 7.2: 77 percent / hydrochloric acid / Heating View Scheme |
Fmoc-Glu(OtBu)-OH
A
L-glutamic acid
B
L-glutamic acid 5-tert-butyl ester
Conditions | Yield |
---|---|
Stage #1: Fmoc-Glu(OtBu)-OH With sodium azide In N,N-dimethyl-formamide at 50℃; for 4h; Stage #2: With piperidine In N,N-dimethyl-formamide | A n/a B 92% |
L-glutamic acid
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran; water at 20℃; for 7h; | 88% |
Conditions | Yield |
---|---|
With 1,4-dihydronicotinamide adenine dinucleotide; ethanol; ammonium chloride; adenosine 5'-diphosphate; L-glutamic dehydrogenase at 30℃; for 2h; tris-acetate buffer, pH 8.5; | 86% |
With ammonium; nicotinamide adenine dinucleotide phosphate; 2-hydroxyethanethiol; GluDH enzymes Mechanism; Irradiation; Tris buffer, 0.1 M, pH 7.9; Ru(bpy)3(2+), 2.2E-5 M as sensitizer; | |
With L-alanin In water at 25℃; Thermodynamic data; Equilibrium constant; biochemical transamination reaction by alanine aminotransferase; further transamination reagents: L-tyrosine, L-phenylalanine and further enzyme; pH 6.60-7.37; standard molar enthalpy, entropy, and Gibbs energy changes; |
hexan-1-amine
(S)-2-(3,5-Dinitro-4-oxo-4H-pyridin-1-yl)-pentanedioic acid
A
L-glutamic acid
B
1-hexyl-3,5-dinitro-4-pyridone
Conditions | Yield |
---|---|
In pyridine Product distribution; | A 84% B n/a |
Boc-Gln(Boc)-Otert.Bu
L-glutamic acid
Conditions | Yield |
---|---|
With trifluoroacetic acid for 0.166667h; Ambient temperature; | 79% |
L-glutamic acid
Conditions | Yield |
---|---|
Stage #1: (S)-5-((1R,5R)-5-Methyl-2,6,8-trioxa-bicyclo[3.2.1]oct-1-yl)-1,5-dihydro-pyrrol-2-one With hydrogenchloride Heating; Stage #2: With Dowex 50W-X8 | 77% |
(5S)-1-tert-butoxycarbonyl-5-(5-methyl-2,7,8-trioxabicyclo[3.2.1]oct-1-yl)-5H-pyrrolin-2-one
L-glutamic acid
Conditions | Yield |
---|---|
Stage #1: (5S)-1-tert-butoxycarbonyl-5-(5-methyl-2,7,8-trioxabicyclo[3.2.1]oct-1-yl)-5H-pyrrolin-2-one With hydrogen; palladium on activated charcoal In methanol Stage #2: With hydrogenchloride Heating; | 77% |
Conditions | Yield |
---|---|
With boron trichloride In dichloromethane at 25℃; for 0.333333h; | 71% |
With sulfuric acid at 50℃; Rate constant; other reaction partner, other temperature; | |
With hydrogen; palladium on activated charcoal In dichloromethane at 20℃; for 24h; atmospheric pressure; | 41 mg |
With ethylenediaminetetraacetic acid; phenylmethylsulphonyl fluoride; water In aq. phosphate buffer at 30℃; Kinetics; Reagent/catalyst; Microbiological reaction; Enzymatic reaction; |
L-glutamic acid
Conditions | Yield |
---|---|
With ruthenium nanoparticles dispersed in a polyvinylpyrrolidone matrix; amberlyst A-21 In methanol; dichloromethane | 68% |
Boc-Gln-OH
trifluoroacetic acid
A
L-glutamic acid
B
L-Pyroglutamic acid
Conditions | Yield |
---|---|
at 20℃; for 0.25h; | A 61% B 18% |
(S)-3-[3-(benzyloxycarbonyl)-5-oxooxazolidin-4-yl]propanoic acid
L-glutamic acid
Conditions | Yield |
---|---|
With boron trichloride In dichloromethane at 25℃; for 0.333333h; | 58% |
Conditions | Yield |
---|---|
With NH4Cl-NH4OH buffer pH 8.5; nickel dichloride at 60℃; for 24h; N-carbamyl-L-amino acid aminohydrolase; | 56% |
With potassium phosphate buffer; Pseudomonas sp. AJ-11220 In various solvent(s) at 30℃; for 1h; | |
With potassium phosphate buffer; Pseudomonas sp. AJ-11220 In various solvent(s) at 30℃; for 1h; pH 7.5; enzymatic reaction; |
L-glutamic acid
Conditions | Yield |
---|---|
Stage #1: (S)-2-((R)-2-Allyloxy-1-phenyl-ethylamino)-pentanedinitrile With palladium dihydroxide; hydrogen In ethanol at 20℃; under 76000 Torr; Stage #2: With hydrogenchloride; water at 100℃; | 20% |
α-ketoglutaric acid
L-alanin
A
L-glutamic acid
B
2-oxo-propionic acid
Conditions | Yield |
---|---|
Gleichgewicht; | |
im lebenden tierischen Organismus; |
α-ketoglutaric acid
L-leucine
A
4-methyl-2-oxopentanoic acid
B
L-glutamic acid
Conditions | Yield |
---|---|
in Gegenwart von Enzym-Praeparaten aus tierischen Geweben; | |
in Gegenwart von Enzym-Praeparaten aus Pflanzen; | |
in Gegenwart von Enzym-Praeparaten aus Torulopsis utilis; | |
With Erwinia carotovora subsp. carotovora aromatic aminotransferase PAT1 Enzymatic reaction; |
α-ketoglutaric acid
L-Cysteic acid
A
L-glutamic acid
B
sulfo-pyruvic acid
Conditions | Yield |
---|---|
in Gegenwart von Transaminase-Praeparaten aus Herzmuskel; |
Conditions | Yield |
---|---|
Einwirkung von Streptococcus-Arten.Hydrolysis; | |
Einwirkung von Proteus vulgaris.Hydrolysis; | |
Einwirkung von Proteus morganii.Hydrolysis; | |
Einwirkung von Staphylococcus.Hydrolysis; | |
Einwirkung von Saccharomyces cerevisiae.Hydrolysis; |
Conditions | Yield |
---|---|
enzymatische Hydrolyse; | |
With Tris-HCl buffer; N74D Escherichia coli asparagine synthetase B mutant; BIS-TRIS; magnesium chloride at 37℃; pH=6.5; Enzyme kinetics; Hydrolysis; | |
With potassium dihydrogenphosphate at 25℃; pH=5.14; Thermodynamic data; Equilibrium constant; Hydrolysis; |
Conditions | Yield |
---|---|
nach Verfuetterung an Kaninchen findet sich im Harn; | |
Bei der Einw. des Schimmelpilzes Penicillium purpurogenum; | |
Einw. von Penicillium glaucum; |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane at 20℃; for 0.25h; Inert atmosphere; | 100% |
With chloro-trimethyl-silane at 20℃; | 97% |
With chloro-trimethyl-silane at 20℃; for 0.166667h; | 97% |
methanol
L-glutamic acid
L-glutamic acid dimethyl ester
Conditions | Yield |
---|---|
With thionyl chloride | 100% |
With chloro-trimethyl-silane at 0 - 10℃; for 15h; | 99.1% |
With thionyl chloride at 0 - 20℃; for 12.5h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
Stage #1: methanol With thionyl chloride at 0℃; for 0.5h; Stage #2: L-glutamic acid at 21℃; for 72h; Inert atmosphere; | 100% |
With chloro-trimethyl-silane at 20℃; | 99% |
With chloro-trimethyl-silane at 20℃; for 16h; | 98% |
L-glutamic acid
4-{[N-[(2,4-diamino-6-pteridinyl)methyl]-N-methyl]amino}benzoyl azide
N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamic acid
Conditions | Yield |
---|---|
With 1,1,3,3-tetramethylguanidine In dimethyl sulfoxide at 25℃; for 1h; Acylation; | 100% |
chloro-trimethyl-silane
L-glutamic acid
L-glutamic dimethyl ester hydrochloride
Conditions | Yield |
---|---|
In methanol at 20℃; for 16h; | 100% |
Conditions | Yield |
---|---|
With triethylamine In water; N,N-dimethyl-formamide for 1h; | 100% |
With triethylamine In water; acetone at 25℃; for 4.5h; | 90% |
Stage #1: L-glutamic acid With sodium hydroxide In water pH=11; Stage #2: di-tert-butyl dicarbonate In tetrahydrofuran; water at 20℃; Cooling; Stage #3: With hydrogenchloride In tetrahydrofuran; water pH=2; | 89% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 5 - 20℃; for 18h; Heating / reflux; | 100% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 5 - 20℃; for 24h; Heating / reflux; | 100% |
L-glutamic acid
Conditions | Yield |
---|---|
Stage #1: L-glutamic acid With magnesium oxide In water at 60℃; for 1h; Stage #2: With magnesium chloride In water | 100% |
Stage #1: L-glutamic acid With magnesium oxide In water at 60℃; for 1h; Stage #2: With magnesium bromide In water | 100% |
L-glutamic acid
1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyridin-1-ium-3-carboxylate
Conditions | Yield |
---|---|
In water pH=3.52; Cooling with ice; | 100% |
Conditions | Yield |
---|---|
In water for 0.166667h; pH=Ca. 2.8 - 3.3; Cooling with ice; | 100% |
Conditions | Yield |
---|---|
In water for 0.25h; | 100% |
In water at 20℃; for 0.25h; |
Conditions | Yield |
---|---|
In methanol at 55℃; for 3h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
Stage #1: L-glutamic acid; tetra(n-butyl)ammonium hydroxide In methanol Stage #2: (S)-1,1-dinaphthalene-2,2'-dicarboxaldehyde In methanol at 20℃; for 72h; Molecular sieve; | 100% |
Conditions | Yield |
---|---|
In neat (no solvent) for 0.166667h; Green chemistry; | 99.5% |
Conditions | Yield |
---|---|
With sulfuric acid In toluene for 24h; Heating; | 99% |
With acetyl chloride at 110℃; for 1h; | |
Reflux; |
L-glutamic acid
chloroformic acid ethyl ester
3-Phenylpropionic acid
A
C8H13NO6
Conditions | Yield |
---|---|
Stage #1: chloroformic acid ethyl ester; 3-Phenylpropionic acid With triethylamine In tetrahydrofuran at 0℃; for 0.5h; Stage #2: L-glutamic acid With sodium hydroxide In tetrahydrofuran; water at 0℃; for 0.5h; pH=7.5; | A n/a B 99% |
Conditions | Yield |
---|---|
In ethanol at 0℃; for 4h; Reflux; | 99% |
L-glutamic acid
benzyl alcohol
L-glutamic acid dibenzyl ester hydrochloride
Conditions | Yield |
---|---|
Stage #1: L-glutamic acid; benzyl alcohol With thionyl chloride at 80 - 85℃; for 5h; Stage #2: With hydrogenchloride at 20 - 25℃; for 0.5h; Concentration; Temperature; Reagent/catalyst; | 98.7% |
With thionyl chloride at 5℃; for 5.33333h; Heating; | 85% |
Stage #1: L-glutamic acid; benzyl alcohol at 20 - 90℃; Stage #2: With sodium carbonate In water pH=10; Stage #3: With hydrogenchloride In diethyl ether |
Conditions | Yield |
---|---|
With triethylamine In methanol for 3h; | 98% |
With sodium hydroxide In water at 0 - 20℃; for 6.5h; | 98% |
In water at 0℃; for 2h; | 96% |
Conditions | Yield |
---|---|
With thionyl chloride at 20℃; for 24h; | 98% |
With thionyl chloride Ambient temperature; | 89% |
Conditions | Yield |
---|---|
With thionyl chloride | 98% |
Stage #1: ethanol; L-glutamic acid With bis(trichloromethyl) carbonate at 70 - 75℃; for 5h; Stage #2: With hydrogenchloride at 20 - 25℃; for 0.5h; | 98% |
Stage #1: ethanol With thionyl chloride at -10 - 10℃; for 1h; Stage #2: L-glutamic acid at 20 - 80℃; for 2h; | 77.76% |
L-glutamic acid
(2S)-tetrahydro-5-oxofuran-2-carboxylic acid
Conditions | Yield |
---|---|
With hydrogenchloride; sodium nitrite In water at 15℃; optical yield given as %ee; | 98% |
With hydrogenchloride; water; sodium nitrite at 0 - 20℃; for 18h; | 92% |
With hydrogenchloride; sodium nitrite In water at -5 - 20℃; Inert atmosphere; | 91.6% |
Conditions | Yield |
---|---|
In water for 0.0666667h; Irradiation; | 98% |
at 0 - 20℃; | 61% |
With water | 58% |
With acetic acid Heating; |
L-glutamic acid
m-nitrobenzoic acid chloride
N-(m-nitrobenzoyl)-L-glutamic acid
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; triethylamine In dichloromethane at 25℃; for 4h; | 98% |
Stage #1: L-glutamic acid With sodium hydrogencarbonate In water Stage #2: m-nitrobenzoic acid chloride In water; benzene at 10℃; for 1h; Further stages.; | |
With sodium carbonate In 1,4-dioxane; water at 20℃; for 12h; |
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