Welcome to LookChem.com Sign In|Join Free

CAS

  • or

87-73-0

Post Buying Request

87-73-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

87-73-0 Usage

Description

Saccharic acid, also called glucaric acid, is a chemical compound with the formulaC6H10O8. It is derived by oxidizing a sugar such as glucose with nitric acid. The salts of saccharic acid are called saccharates.

Definition

ChEBI: D-glucaric acid is the D-enantiomer of glucaric acid. It has a role as an antineoplastic agent. It is a conjugate acid of a D-glucarate(1-). It is an enantiomer of a L-glucaric acid.

Check Digit Verification of cas no

The CAS Registry Mumber 87-73-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87-73:
(4*8)+(3*7)+(2*7)+(1*3)=70
70 % 10 = 0
So 87-73-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O8/c7-1(3(9)5(11)12)2(8)4(10)6(13)14/h1-4,7-10H,(H,11,12)(H,13,14)/t1-,2-,3-,4+/m0/s1

87-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name D-glucaric acid

1.2 Other means of identification

Product number -
Other names D-Glu(OtBu)-OH

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:87-73-0 SDS

87-73-0Synthetic route

D-glucose
50-99-7

D-glucose

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
With 5 % platinum on carbon; oxygen In water at 80℃; under 10351 Torr; for 10h; pH=7.2; pH-value; Temperature; Pressure;74%
With oxygen In water at 110℃; under 8517.48 Torr; for 2h;21%
With nitric acid
D-glucaric acid monopotassium salt
576-42-1

D-glucaric acid monopotassium salt

A

D-glucaric acid
87-73-0

D-glucaric acid

B

D-Glucaro-1,4-lacton
389-36-6

D-Glucaro-1,4-lacton

C

D-glucaro-6,3-lactone
2782-04-9

D-glucaro-6,3-lactone

Conditions
ConditionsYield
With H(1+) resin Rexyn 100(H) In water for 3h; lactonization;A n/a
B n/a
C 69.1%
D-Glucose
2280-44-6

D-Glucose

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
With 2.44 wt.% platinum and 2.38 wt.% aurum on carbon; oxygen In water at 90℃; under 4635.46 Torr; for 5h; Reagent/catalyst;60%
D-glucose
50-99-7

D-glucose

A

formic acid
64-18-6

formic acid

B

gluconic acid
526-95-4

gluconic acid

C

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
With dihydrogen peroxide; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate In water at 60℃; for 18h;A 7%
B 35%
C 17%
With oxygen; potassium hydrogen phthalate In water for 3h; pH=4.01; Catalytic behavior; Kinetics; Mechanism; Reagent/catalyst; pH-value; UV-irradiation;
D-glucose
50-99-7

D-glucose

A

gluconic acid
526-95-4

gluconic acid

B

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
With oxygen; sodium hydroxide In water at 60℃; under 7500.75 Torr; for 24h; Catalytic behavior; Temperature; Pressure; Reagent/catalyst; Autoclave;A 31%
B 18%
With MoO5; dihydrogen peroxide; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate In water at 60℃; for 18h;A 27%
B 13%
With ammonium vanadate In sulfuric acid at 90℃; for 3h; Kinetics; Mechanism; Equilibrium constant; activation energy; different concentrations of H2SO4;
With oxygen; sodium nitrite In sulfolane; perchloric acid at 59.85℃; under 750.06 Torr; Kinetics; Further Variations:; Temperatures; Pressures;
With Fe-doped TiO2-supported zeolite; air In water; acetonitrile at 30℃; under 760.051 Torr; for 1.5h; Reagent/catalyst; Solvent; UV-irradiation;
gluconic acid
526-95-4

gluconic acid

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
With nitric acid
Bildung aus subcutan injizierte d-Gluconsaeure im Organismus des Kaninchens. (Schott konnte diese Bildung nicht bestaetigen);
With UDP-glucose dehydrogenase Enzymatic reaction;
With sodium sulfate at 25℃; Electrochemical reaction;
gluconic acid
20246-33-7

gluconic acid

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
With nitric acid
Conditions
ConditionsYield
Desaminierung und nachfolgende Oxydation mit Salpetersaeure;
Sucrose
57-50-1

Sucrose

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
With nitric acid
With nitric acid in mehreren Stufen;
With iron(II) ammonium sulfate; disodium hydrogenphosphate; phosphoglucomutase; sucrose phosphorylase; myo-inositol monophosphatase; uronate dehydrogenase; myo-inositol 1-phosphate synthase; myo-inositol oxygenase; nicotinamide adenine dinucleotide oxidase; nicotinamide adenine dinucleotide; magnesium chloride In aq. buffer at 30℃; for 12h; pH=7.5; pH-value; Temperature; Solvent; Concentration; Enzymatic reaction;
D-(+)-lactose
63-42-3

D-(+)-lactose

A

D-glucaric acid
87-73-0

D-glucaric acid

B

meso-galactaric acid
526-99-8, 1213827-87-2

meso-galactaric acid

Conditions
ConditionsYield
With nitric acid
D-raffinose
512-69-6

D-raffinose

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
With nitric acid
Conditions
ConditionsYield
With dihydrogen peroxide; iron(II) sulfate at 30℃; for 1h; Product distribution; Mechanism; effect of reaction time, inhibitors (D-mannitol, thiourea, Me2SO), pH, buffers, further iron salt and complexing agents (EDTA, DTPA, ADP); experiments with a rat-liver microsomal preparation;
With sodium hydroxide; sodium perchlorate; chloroamine-T at 35℃; for 24h; Rate constant; Mechanism; Thermodynamic data; effect of reagents concentration, solvent isotope effect, Ea, ΔH(excit.), ΔS(excit.), ΔG(excit.), also in solvents; effect of reaction products: p-toluensulphonamide and chloride ions;
With dihydrogen peroxide; iron(II) sulfate at 30℃; for 3h; pH 6.0;
With sodium hydroxide; sodium perchlorate; chloramine-B In water at 35℃; Kinetics; Further Variations:; Solvents; Temperatures; ionic strength; Oxidation;
gluconic acid
526-95-4

gluconic acid

A

fructonic acid
669-90-9

fructonic acid

B

α-L-guluronic acid
1986-15-8

α-L-guluronic acid

C

D-glucaric acid
87-73-0

D-glucaric acid

D

oxalic acid
144-62-7

oxalic acid

Conditions
ConditionsYield
With oxygen In water at 55℃; under 750.06 Torr; Product distribution; Mechanism; further catalyst, further reagent, effect of further catalyst and reagent;
sodium 1-deoxy-1-<(N-acetyl-N-phenylamino)oxy>-β-D-glucopyranuronate
13214-42-1

sodium 1-deoxy-1-<(N-acetyl-N-phenylamino)oxy>-β-D-glucopyranuronate

A

D-glucaric acid
87-73-0

D-glucaric acid

B

aniline
62-53-3

aniline

Conditions
ConditionsYield
With sulfuric acid In ethanol at 20℃; Mechanism; Rate constant;
octyl alpha-D-glucopyranoside
29781-80-4

octyl alpha-D-glucopyranoside

A

tartronic acid
80-69-3

tartronic acid

B

meso-tartaric acid
147-73-9

meso-tartaric acid

C

L-Tartaric acid
87-69-4

L-Tartaric acid

D

gluconic acid
526-95-4

gluconic acid

E

D-glucaric acid
87-73-0

D-glucaric acid

F

oxalic acid
144-62-7

oxalic acid

Conditions
ConditionsYield
With oxygen; platinum on activated charcoal In water at 49.9℃; under 300.02 Torr; Product distribution; Mechanism; initial rate of consumption, pH effect;
methyl-alpha-D-glucopyranoside
97-30-3

methyl-alpha-D-glucopyranoside

A

formic acid
64-18-6

formic acid

B

glycolic Acid
79-14-1

glycolic Acid

C

methyl α-D-gluco-hexodialdo-1,5-pyranoside
23598-27-8

methyl α-D-gluco-hexodialdo-1,5-pyranoside

D

methyl α-D-glucopyranosiduronic acid
5155-45-3

methyl α-D-glucopyranosiduronic acid

E

D-erythronic acid
488-16-4

D-erythronic acid

F

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
With oxygen; platinum on activated charcoal In water at 49.9℃; under 300.02 Torr; Product distribution; Mechanism; initial rate of consumption, pH effect;
Conditions
ConditionsYield
With phosphate buffer; dihydrogen peroxide; iron(II) sulfate In water at 37℃; for 6h; pH=7.4; Product distribution; Further Variations:; Reagents; Oxidation;
water
7732-18-5

water

D-Glucaro-1,4-lacton
389-36-6

D-Glucaro-1,4-lacton

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
at 18℃; Rate constant; Hydrolysis;
at 18℃; Equilibrium constant; Hydrolysis;
water
7732-18-5

water

D-glucaro-6,3-lactone
2782-04-9

D-glucaro-6,3-lactone

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
at 18℃; Rate constant; Hydrolysis;
at 18℃; Equilibrium constant; Hydrolysis;
ricestarch

ricestarch

A

D-glucaric acid
87-73-0

D-glucaric acid

B

oxalic acid
144-62-7

oxalic acid

Conditions
ConditionsYield
With nitric acid at 100℃;
water
7732-18-5

water

O2,O5-diacetyl-glucaric acid-1=>4;6=>3-dilactone
1219325-97-9

O2,O5-diacetyl-glucaric acid-1=>4;6=>3-dilactone

A

D-glucaric acid
87-73-0

D-glucaric acid

B

acetic acid
64-19-7

acetic acid

Conditions
ConditionsYield
Hydrolysis; O2,O5-diacetyl-glucaric acid-1=>4;6=>3-dilactone;
D-glucose
50-99-7

D-glucose

nitric acid
7697-37-2

nitric acid

D-glucaric acid
87-73-0

D-glucaric acid

gluconic acid
526-95-4

gluconic acid

nitric acid
7697-37-2

nitric acid

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
at 85℃;
gluconic acid
20246-33-7

gluconic acid

nitric acid
7697-37-2

nitric acid

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
das Lacton reagiert;
gluconic acid
526-95-4

gluconic acid

dinitrogen tetraoxide
10544-72-6

dinitrogen tetraoxide

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
at 25℃;
tetrachloromethane
56-23-5

tetrachloromethane

gluconic acid
526-95-4

gluconic acid

dinitrogen tetraoxide
10544-72-6

dinitrogen tetraoxide

D-glucaric acid
87-73-0

D-glucaric acid

Conditions
ConditionsYield
at 25℃;
methanol
67-56-1

methanol

D-glucaric acid
87-73-0

D-glucaric acid

hexanedioic acid dimethyl ester
627-93-0

hexanedioic acid dimethyl ester

Conditions
ConditionsYield
With potassium perrhenate; phosphoric acid; palladium on activated charcoal; hydrogen; pyrographite at 150℃; under 3878.71 Torr;85%
D-glucaric acid
87-73-0

D-glucaric acid

furan-2,5-dicarboxylic acid
3238-40-2

furan-2,5-dicarboxylic acid

Conditions
ConditionsYield
With benzenesulfonic acid for 0.0333333h; microwave irradiation;58%
With toluene-4-sulfonic acid at 140℃; for 2h;52%
With 1-butyl-3-methylimidazolium hydrogen sulfate; sulfuric acid at 120℃; for 17h; Temperature;39 %Chromat.
With sulfolane; sulfuric acid In toluene at 100 - 130℃; Reagent/catalyst; Solvent; Temperature;
D-glucaric acid
87-73-0

D-glucaric acid

Lg-threo-4-hydroxy-2,5-dimethoxy-hex-2c-enedioic acid-1-lactone-6-methyl ester
4041-92-3

Lg-threo-4-hydroxy-2,5-dimethoxy-hex-2c-enedioic acid-1-lactone-6-methyl ester

Conditions
ConditionsYield
With diethyl ether
formaldehyd
50-00-0

formaldehyd

D-glucaric acid
87-73-0

D-glucaric acid

4,5-bis-(5-oxo-[1,3]dioxolan-4-yl)-[1,3]dioxolane

4,5-bis-(5-oxo-[1,3]dioxolan-4-yl)-[1,3]dioxolane

Conditions
ConditionsYield
bei 10-20-maligem Abdampfen; -β.β'-methylene ether α.α'-bis-methylene ether ester;
1-amino-3-methylbutane
107-85-7

1-amino-3-methylbutane

D-glucaric acid
87-73-0

D-glucaric acid

1-(3-methyl-butyl)-pyrrole
13679-79-3

1-(3-methyl-butyl)-pyrrole

Conditions
ConditionsYield
under 70 Torr; bei der Destillation;
D-glucose
50-99-7

D-glucose

D-glucaric acid
87-73-0

D-glucaric acid

L-Tartaric acid
87-69-4

L-Tartaric acid

Conditions
ConditionsYield
With nitric acid waehrend aus Staerke;
D-glucaric acid
87-73-0

D-glucaric acid

phenylhydrazine hydrochloride
59-88-1

phenylhydrazine hydrochloride

idaric acid bis-(N'-phenyl-hydrazide)
7404-38-8, 99782-61-3, 110507-66-9

idaric acid bis-(N'-phenyl-hydrazide)

Conditions
ConditionsYield
With sodium acetate -bis-phenylhydrazide;
D-glucaric acid
87-73-0

D-glucaric acid

A

3-hydroxy-2-pyrone
496-64-0

3-hydroxy-2-pyrone

B

2-furanoic acid
88-14-2

2-furanoic acid

Conditions
ConditionsYield
With potassium pyrosulfate
D-glucaric acid
87-73-0

D-glucaric acid

A

4H-pyran-2,3-dione

4H-pyran-2,3-dione

B

2-furanoic acid
88-14-2

2-furanoic acid

Conditions
ConditionsYield
With potassium pyrosulfate
D-glucaric acid
87-73-0

D-glucaric acid

Adipic acid
124-04-9

Adipic acid

Conditions
ConditionsYield
With phosphorus; hydrogen iodide at 140 - 150℃; im geschlossenen Rohr;
With hydrogen iodide; hydrogen In acetic acid at 210℃; for 3h; Flow reactor;
D-glucaric acid
87-73-0

D-glucaric acid

L-Tartaric acid
87-69-4

L-Tartaric acid

Conditions
ConditionsYield
With permanganate(VII) ion at 0℃;
With sulfuric acid Electrolysis;
With dihydrogen peroxide
D-glucaric acid
87-73-0

D-glucaric acid

A

L-Tartaric acid
87-69-4

L-Tartaric acid

DL-tartaric acid
133-37-9

DL-tartaric acid

Conditions
ConditionsYield
With nitric acid
D-glucaric acid
87-73-0

D-glucaric acid

DL-tartaric acid
133-37-9

DL-tartaric acid

Conditions
ConditionsYield
With nitric acid
D-glucaric acid
87-73-0

D-glucaric acid

2-acetoacetic acid
541-50-4

2-acetoacetic acid

Conditions
ConditionsYield
bei der Durchblutung der ueberlebenden Leber;
D-glucaric acid
87-73-0

D-glucaric acid

succinic acid
110-15-6

succinic acid

Conditions
ConditionsYield
bei der Einw.von Bac.coli unter anaeroben Bedingungen;
With calcium carbonate bei der Einw.von Bact.lactis aerogenes unter anaeroben Bedingungen;
D-glucaric acid
87-73-0

D-glucaric acid

4,5-bis-phenylhydrazono-L-threo-4,5-dideoxy-pentonic acid

4,5-bis-phenylhydrazono-L-threo-4,5-dideoxy-pentonic acid

Conditions
ConditionsYield
Reaktion ueber mehrere Stufen;
D-glucaric acid
87-73-0

D-glucaric acid

D-glucurono-6,3-lactone
32449-92-6

D-glucurono-6,3-lactone

Conditions
ConditionsYield
With sodium amalgam; sulfuric acid; water
D-glucaric acid
87-73-0

D-glucaric acid

A

D-Glucaro-1,4-lacton
389-36-6

D-Glucaro-1,4-lacton

B

D-glucaro-6,3-lactone
2782-04-9

D-glucaro-6,3-lactone

Conditions
ConditionsYield
Eindampfen einer wss. Loesung unter vermindertem Druck;
D-glucaric acid
87-73-0

D-glucaric acid

(3-hydroxy-5-oxo-4-phenylhydrazono-tetrahydro-[2]furyl)-phenylhydrazono-acetic acid

(3-hydroxy-5-oxo-4-phenylhydrazono-tetrahydro-[2]furyl)-phenylhydrazono-acetic acid

Conditions
ConditionsYield
With water; dihydrogen peroxide; iron man faellt mit Phenylhydrazinacetat; bis-phenylhydrazone of melting point 242 degree-244 degree;
D-glucaric acid
87-73-0

D-glucaric acid

acetic anhydride
108-24-7

acetic anhydride

O2,O5-diacetyl-glucaric acid-1=>4;6=>3-dilactone
1219325-97-9

O2,O5-diacetyl-glucaric acid-1=>4;6=>3-dilactone

Conditions
ConditionsYield
With zinc(II) chloride O2,O5-diacetyl-glucaric acid-1=>4;6=>3-dilactone;

87-73-0Relevant articles and documents

Catalytic wet air oxidation of D-glucose by perovskite type oxides (Fe, Co, Mn) for the synthesis of value-added chemicals

Geobaldo, Francesco,Pirone, Raffaele,Russo, Nunzio,Scelfo, Simone

, (2022/03/15)

The conversion of common biomasses derived, as D-glucose, into value-added chemicals has received highest attention in the last few years. Among all processes, the catalytic wet air oxidation (CWAO) of derived biomasses using noble metal-based heterogeneo

Boosting electrocatalytic nitrogen fixation: Via energy-efficient anodic oxidation of sodium gluconate

Zhao, Lu,Kuang, Xuan,Chen, Cheng,Sun, Xu,Wang, Zhiling,Wei, Qin

supporting information, p. 10170 - 10173 (2019/08/30)

Here, we report an anodic replacement of the water oxidation reaction with more readily oxidizable species to facilitate ambient electrocatalytic nitrogen reduction reaction (NRR). A self-supported catalyst, CuII-MOF on carbon cloth (JUC-1000/CC), acts as a versatile cathode and anode for both NRR and electro-oxidation of sodium gluconate to glucaric acid. Impressively, the two-electrode system requires a potential of only 0.4 V to achieve an NH3 yield rate of 24.7 μg h-1 mgcat-1, an FE of 11.90% and an SA selectivity of 96.96%, and shows strong electrochemical stability. This study reveals that the strategy avoids the sacrifice of the NH3 yield to increase FE, and offers an efficient and simultaneous electrosynthesis of NH3 and SA.

Enhanced photocatalytic performance for oxidation of glucose to value-added organic acids in water using iron thioporphyrazine modified SnO2

Zhang, Quanquan,Ge, Yanchun,Yang, Changjun,Zhang, Bingguang,Deng, Kejian

supporting information, p. 5019 - 5029 (2019/09/30)

The selective conversion of glucose into value-added chemicals in the presence of only water is a challenging topic. In this work, selective photocatalytic oxidation of glucose in water was studied using iron thioporphyrazine modified SnO2 (SnO2/FePz(SBu)8) as the catalyst and atmospheric air as the oxidant under simulated sunlight irradiation. It was found that value-added organic acids including glucaric acid, gluconic acid and formic acid could be obtained from the oxidation of glucose under such conditions. The effects of the FePz(SBu)8 content, glucose concentration and additional addition on the conversion of glucose and the selectivity of the organic acids were further explored. Under the optimized conditions, the total selectivity for the organic acids on the SnO2/FePz(SBu)8 photocatalyst reached up to 52.2% at 34.2% glucose conversion. More importantly, it has been demonstrated that the presence of FePz(SBu)8 on the surface of SnO2 can keep the selectivity of the organic acids unchanged under conditions of increasing the glucose conversion. To illustrate the synergistic effect for the enhanced photocatalytic activity between FePz(SBu)8 and SnO2, surface photocurrent, electron spin resonance (ESR) spectra and adsorption behavior experiments were carried out on pure SnO2 and SnO2/FePz(SBu)8. It was found that the introduction of FePz(SBu)8 could enhance the separation of photogenerated charge, promote the generation of active species for photocatalysis and improve the adsorption capacity of glucose, which are beneficial to the enhancement of photocatalytic activity. Additionally, a possible pathway of glucose oxidation was proposed through both detailed analysis of the oxidation intermediate of glucose and comparative experiments with different organic acids as the substrates, indicating that the formation of organic acids were fulfilled by two parallel and subsequent reactions at the beginning of the reaction.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 87-73-0