D-Glucuronic acid supplier | CasNO.6556-12-3

Name
D-Glucuronic acid
EINECS 229-486-4
CAS No. 6556-12-3
Article Data202
CAS DataBase
Density 1.987 g/cm³
Solubility very soluble in water
Melting Point 159-161 °C(lit.)
Formula C₆H₁₀O₇
Boiling Point 495.2 °C at 760 mmHg
Molecular Weight 194.141
Flash Point 211.1 °C
Transport Information
Appearance White Solid
Safety 37/39-26-36
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Glucuronicacid, D- (8CI);D-(+)-Glucuronic acid;Glucosiduronic acid;Glucuronic acid;
PSA 135.29000
LogP -3.28650

Synthetic route

: apigenin 7-O-[β-D-glucuronopyranosyl-(1->2)]-O-β-D-glucuronopyranoside

A: 6556-12-3
D-Glucuronic acid

B: 520-36-5
5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

Conditions

Conditions	Yield
Acid hydrolysis;	A n/a B 52%

: 97-30-3
methyl-alpha-D-glucopyranoside

: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With sulfuric acid; water; sodium sulfate under 8090.6 Torr; Electrolysis.anschl. Erwaermen mit wss. H2SO4;
With platinum on activated charcoal; water; sodium hydrogencarbonate unter Einleiten von Luft und anschl. Behandeln mit wss. H2SO4;
With water; nitric acid; sodium nitrite anschl. Erwaermen mir wss. H2SO4;
With chloroform; dinitrogen tetraoxide anschl. mit wss. H2SO4;
With tetrachloromethane; dinitrogen tetraoxide anschl. mit wss. Methanol und dann mit wss. H2SO4;

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

: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With barium dihydroxide; water
With alkaline solution; water

: 79466-08-3
(-)-Menthol glucuronide

: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With sulfuric acid; water anschl. Erwaermen mit BaCO3, dann mit wss.-aethanol. H2SO4;

: C55H90O23

A: 3615-41-6
L-Rhamnose

B: 50-99-7
D-glucose

C: 59-23-4
D-Galactose

D: 6556-12-3
D-Glucuronic acid

E: 2611-08-7, 53342-82-8
Protoprimulagenin A

Conditions

Conditions	Yield
With hydrogenchloride for 2h; Heating;

...Expand

: echinocystic acid 3-O-β-D-glucuronopyranoside

A: 6556-12-3
D-Glucuronic acid

B: 510-30-5
echinocystic acid

Conditions

Conditions	Yield
With hydrogenchloride for 2h;

: foetidissimoside A

A: 58-86-6
D-xylose

B: 6556-12-3
D-Glucuronic acid

C: C41H66O12

Conditions

Conditions	Yield
With β-glucuronidase; sodium acetate; acetic acid at 39℃; for 48h;

...Expand

: C47H76O20

A: 5328-37-0
L-arabinose

B: 50-99-7
D-glucose

C: 6556-12-3
D-Glucuronic acid

D: 15448-03-0
A1-barrigenol

Conditions

Conditions	Yield
With hydrogenchloride; silver carbonate In methanol for 2h;

...Expand

: C47H76O21

A: 5328-37-0
L-arabinose

B: 6556-12-3
D-Glucuronic acid

C: 15448-03-0
A1-barrigenol

Conditions

Conditions	Yield
With hydrogenchloride; silver carbonate In methanol for 2h;

...Expand

: A1-barrigenol 3-O-β-D-glucopyranosyl-(1 - 2)-<β-D-galactopyranosyl-(1 - 3)>-β-D-glucopyranosiduronic acid

A: 3458-28-4
D-Mannose

B: 50-99-7
D-glucose

C: 6556-12-3
D-Glucuronic acid

D: 15448-03-0
A1-barrigenol

Conditions

Conditions	Yield
With sulfuric acid In ethanol for 2h;

...Expand

: C53H86O25

A: 5328-37-0
L-arabinose

B: 50-99-7
D-glucose

C: 6556-12-3
D-Glucuronic acid

D: 15448-03-0
A1-barrigenol

Conditions

Conditions	Yield
With hydrogenchloride; silver carbonate In methanol for 2h;

...Expand

calcium salt of/the/ O1,O2-isopropylidene-α-D-glucofuranuronic acid: calcium salt of/the/ O1,O2-isopropylidene-α-D-glucofuranuronic acid

: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With water; oxalic acid

D-glucaric acid-1->4-lactone hydrate: D-glucaric acid-1->4-lactone hydrate

: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With sodium amalgam; water

d-saccharolactonic acid: d-saccharolactonic acid

: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With sodium amalgam; water

euxanthinic acid: euxanthinic acid

: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With water at 120 - 125℃;
With sulfuric acid at 135℃; im Autoklaven;

mentholglucuronic acid: mentholglucuronic acid

: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With sulfuric acid

O1-<(Ξ)-bornyl>-β-D-glucopyranuronic acid: O1-<(Ξ)-bornyl>-β-D-glucopyranuronic acid

: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With sulfuric acid; water

: 50-99-7
D-glucose

: 147-79-5, 304-59-6, 15490-42-3
rochelle salt

copper (II)-hydroxide: copper (II)-hydroxide

aqueous NaOH-solution: aqueous NaOH-solution

A: 849585-22-4
LACTIC ACID

B: 80-69-3
tartronic acid

C: 526-95-4
gluconic acid

D: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
Produkt 5: Acetaldehyd;

...Expand

: 50-99-7
D-glucose

: 7732-18-5
water

A: 526-95-4
gluconic acid

B: 6556-12-3
D-Glucuronic acid

C: 131543-46-9
Glyoxal

Conditions

Conditions	Yield
bei der Einwirkung von γ-Strahlen unter Durchleiten von Sauerstoff.Irradiation;

...Expand

: 3-O-{β-D-apiofuranosyl-(1->4)-[α-L-arabinopyranosyl-(1->2)]-β-D-glucuronopyranosyl}oleanolic acid

A: 639-97-4, 6477-44-7, 42927-70-8
D-apiose

B: 59-23-4
D-Galactose

C: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 100℃; for 1h;

...Expand

: 3-O-{α-L-ramnopyranosyl-(1->4)-[α-L-arabinopyranosyl-(1->2)]-β-D-glucuronopyranosyl}oleanolic acid

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

C: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 100℃; for 1h;

...Expand

: 3-O-[β-D-apiofuranosyl-(1->4)-β-D-glucuronopyranosyl]oleanolic acid 28-O-β-D-glucopyranosyl ester

A: 639-97-4, 6477-44-7, 42927-70-8
D-apiose

B: 50-99-7
D-glucose

C: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 100℃; for 1h;

...Expand

: 3-O-{α-L-rhamnopyranosyl-(1->4)-[β-D-galactopyranosyl-(1->2)]-β-D-glucuronopyranosyl}oleanolic acid

A: 3615-41-6
L-Rhamnose

B: 59-23-4
D-Galactose

C: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 100℃; for 1h;

...Expand

: 3-O-{β-D-apiofuranosyl-(1->4)-[α-L-arabinopyranosyl-(1->2)]-β-D-glucuronopyranosyl}oleanolic acid 28-O-β-D-glucopyranosyl ester

A: 639-97-4, 6477-44-7, 42927-70-8
D-apiose

B: 5328-37-0
L-arabinose

C: 50-99-7
D-glucose

D: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 100℃; for 1h;

...Expand

: 3-O-{α-L-rhamnopyranosyl-(1->4)-[α-L-arabinopyranosyl-(1->2)]-β-D-glucuronopyranosyl}oleanolic acid 28-O-β-D-glucopyranosyl ester

A: 5328-37-0
L-arabinose

B: 3615-41-6
L-Rhamnose

C: 50-99-7
D-glucose

D: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 100℃; for 1h;

...Expand

: 3-O-{α-L-rhamnopyranosyl-(1->4)-[β-D-galactopyranosyl-(1->2)]-β-D-glucuronopyranosyl}oleanolic acid 28-O-β-D-glucopyranosyl ester

A: 3615-41-6
L-Rhamnose

B: 50-99-7
D-glucose

C: 59-23-4
D-Galactose

D: 6556-12-3
D-Glucuronic acid

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane at 100℃; for 1h;

...Expand

: 2280-44-6
D-Glucose

A: 526-95-4
gluconic acid

B: 6556-12-3
D-Glucuronic acid

C: 87-73-0
D-glucaric acid

D: 3056-44-8
glucose dialdehyde

Conditions

Conditions	Yield
With sodium hydroxide; oxygen In water at 60℃; pH=9;

...Expand

: desacyl yuchasaponin A

A: 3615-41-6
L-Rhamnose

B: 50-99-7
D-glucose

C: 59-23-4
D-Galactose

D: 6556-12-3
D-Glucuronic acid

E: 15399-43-6
R1-barrigenol

Conditions

Conditions	Yield
With sulfuric acid; water In 1,4-dioxane for 2h; Reflux;

...Expand

: C54H88O26

A: 3615-41-6
L-Rhamnose

B: 59-23-4
D-Galactose

C: 6556-12-3
D-Glucuronic acid

D: 15399-43-6
R1-barrigenol

Conditions

Conditions	Yield
With sulfuric acid; water In 1,4-dioxane for 2h; Reflux;

...Expand

: 6556-12-3
D-Glucuronic acid

: 771-97-1
2,3-Diaminonaphthalene

: 1027103-31-6
(1'S,2'R,3'R,4'R)-2-[4'-carboxy-1',2',3',4'-tetrahydroxypentyl]-1H-naphthimidazole

Conditions

Conditions	Yield
With air; iodine; acetic acid at 20℃; for 6h;	97%

: 6556-12-3
D-Glucuronic acid

: 1044642-88-7
tegaserod

: 3-(5-methoxy-1H-indol-3-ylmethylene)-N-pentylcarbazimidamide glucuronate

Conditions

Conditions	Yield
In methanol at 20 - 55℃;	94.7%

: 6556-12-3
D-Glucuronic acid

: 108-24-7
acetic anhydride

: 82970-25-0
2,3,4-tri-O-acetyl-β-D-glucopyranurono-6,1-lactone

Conditions

Conditions	Yield
With iodine at 115℃; for 0.166667h; microwave irradiation;	92%

: 6556-12-3
D-Glucuronic acid

: 1246842-76-1
3-azidopropyl (β-D-galactopyranosyl)-(1→4)-O-2-deoxy-2-acetamido-β-D-glucopyranoside

: 3-azidopropyl β-D-glucopyranosyluronic-(1→3)-β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranoside

Conditions

Conditions	Yield
With Bifidobacterium longum UDP-sugar pyrophosphorylase; human β1−3-glucuronyltransferase; recombinant Arabidopsis thaliana glucuronokinase; UTP; ATP; manganese(ll) chloride In aq. buffer at 37℃; pH=8; Enzymatic reaction;	92%

: 6556-12-3
D-Glucuronic acid

: 3-azidopropyl β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→6)-[2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→2)]-α-D-mannopyranoside

: 3-azidopropyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→2)-[β-D-glucopyranosyluronic-(1→3)-β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→6)]-α-D-mannopyranoside

Conditions

Conditions	Yield
With Bifidobacterium longum UDP-sugar pyrophosphorylase; human β1−3-glucuronyltransferase; recombinant Arabidopsis thaliana glucuronokinase; UTP; ATP; manganese(ll) chloride In aq. buffer at 37℃; pH=8; Enzymatic reaction;	91%

: 6556-12-3
D-Glucuronic acid

: 3-azidopropyl β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→2)-β-D-mannopyranoside

: 3-azidopropyl β-D-glucopyranosyluronic-(1→3)-β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→2)-α-D-mannopyranoside

Conditions

Conditions	Yield
With Bifidobacterium longum UDP-sugar pyrophosphorylase; human β1−3-glucuronyltransferase; recombinant Arabidopsis thaliana glucuronokinase; UTP; ATP; manganese(ll) chloride In aq. buffer at 37℃; pH=8; Enzymatic reaction;	91%

: 6556-12-3
D-Glucuronic acid

: 3-azidopropyl β-D-glucopyranosyluronic-(1→3)-β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→2)[2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→6)]-α-D-mannopyranoside

: 3-azidopropyl β-D-glucopyranosyluronic-(1→3)-β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→2)[β-D-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→6)]-α-D-mannopyranoside

Conditions

Conditions	Yield
With Bifidobacterium longum UDP-sugar pyrophosphorylase; human β1−3-glucuronyltransferase; recombinant Arabidopsis thaliana glucuronokinase; UTP; ATP; manganese(ll) chloride In aq. buffer at 37℃; pH=8; Enzymatic reaction;	90%

: 6556-12-3
D-Glucuronic acid

: acetamido cetyl dimethyl ammonium hydroxide

: acetamido cetyl dimethyl ammonium glucuronate

Conditions

Conditions	Yield
In methanol at 20℃; for 1.5h;	86%

: 6556-12-3
D-Glucuronic acid

: ethyl β-D-galactopyranosyl-(1→4)-2-deoxy-2-trifluoroacetamido-1-thio-β-D-glucopyranoside

: ethyl β-D-glucopyranosyluronate-(1→3)-β-D-galactopyranosyl-(1→4)-2-deoxy-2-trifluoroacetamido-1-thio-β-D-glucopyranoside

Conditions

Conditions	Yield
With Bifidobacterium longum UDP-sugar pyrophosphorylase; human β1−3-glucuronyltransferase; recombinant Arabidopsis thaliana glucuronokinase; UTP; ATP; manganese(ll) chloride In aq. buffer at 37℃; pH=8; Enzymatic reaction;	82%

: 6556-12-3
D-Glucuronic acid

: 100-39-0
benzyl bromide

: benzyl α,β-D-glucuronate

Conditions

Conditions	Yield
With tetrabutyl ammonium fluoride In tetrahydrofuran; N,N-dimethyl-formamide at 0 - 20℃; for 18h; Inert atmosphere;	72.6%

: 6556-12-3
D-Glucuronic acid

: 111-26-2
hexan-1-amine

: 1115231-03-2
1-(N-hexyl)glucaric acid monoamide

Conditions

Conditions	Yield
With iodine; potassium carbonate In methanol at 20℃; for 12h;	61%

: 111-87-5
octanol

: 6556-12-3
D-Glucuronic acid

: n-octyl β-D-glucofuranosidurono-6,3-lactone

Conditions

Conditions	Yield
With iron(III) chloride In tetrahydrofuran at 20℃; for 24h;	50%

: 6556-12-3
D-Glucuronic acid

: 112-43-6
10-Undecen-1-ol

: (3R,3aR,5R,6R,6aR)-3,6-Dihydroxy-5-undec-10-enyloxy-tetrahydro-furo[3,2-b]furan-2-one

Conditions

Conditions	Yield
With iron(III) chloride In tetrahydrofuran at 20℃; for 72h;	50%

: 6556-12-3
D-Glucuronic acid

: 64-18-6
formic acid

Conditions

Conditions	Yield
With phosphovanadomolybdic acid; oxygen In water at 150℃; under 15001.5 Torr; for 3h;	34.6%

: 6556-12-3
D-Glucuronic acid

: 79-14-1
glycolic Acid

Conditions

Conditions	Yield
With phosphomolybdic acid; oxygen In water at 150℃; under 15001.5 Torr; for 1h; Autoclave;	25.3%

: 3144-74-9
chloromethyldimethylsilane

: 6556-12-3
D-Glucuronic acid

: 19126-97-7
D-glucuronic acid TMS

Conditions

Conditions	Yield
With pyridine; hexane; formamide

: 54-85-3
isoniazid

: 6556-12-3
D-Glucuronic acid

: 111617-78-8
6-isonicotinoylhydrazono-6-deoxy-L-gulonic acid-(N'-isonicotinoyl-hydrazide)

Conditions

Conditions	Yield
With acetic acid

: 54-85-3
isoniazid

: 6556-12-3
D-Glucuronic acid

: 25019-85-6
6-isonicotinoylhydrazono-6-deoxy-L-gulonic acid

Conditions

Conditions	Yield
With water

: 6556-12-3
D-Glucuronic acid

: 132-86-5
1,3-dihydroxynaphthalene

: 103820-48-0
9-methoxy-14-(3-methoxy-2-oxo-2H-pyran-6-yl)-dibenzo[a,j]xanthen-5-one

Conditions

Conditions	Yield
With hydrogenchloride Behandeln des Reaktionsprodukts mit Diazomethan in Aether;

: 6556-12-3
D-Glucuronic acid

: 20605-40-7
thiobenzoylhydrazine

: (S)-((2R)-3c,4c-dihydroxy-5-oxo-tetrahydro-[2r]furyl)-hydroxy-acetaldehyde-thiobenzoylhydrazone

Conditions

Conditions	Yield
With hydrogenchloride

: 6556-12-3
D-Glucuronic acid

: 13148-15-7
2-phenylnaphthalene-1,3-diol

: 4-[(2,4-dihydroxy-3-phenyl-[1]naphthyl)-[2]furyl-methylene]-3-hydroxy-2-phenyl-4H-naphthalen-1-one

Conditions

Conditions	Yield
With acetic acid; zinc(II) chloride

: 6556-12-3
D-Glucuronic acid

: 2937-05-5
4-nitrobenzenesulfonohydrazide

: (S)-((2R)-3c,4c-dihydroxy-5-oxo-tetrahydro-[2r]furyl)-hydroxy-acetaldehyde-(4-nitro-benzenesulfonylhydrazone)

Conditions

Conditions	Yield
With acetonitrile

: 6556-12-3
D-Glucuronic acid

: 151-50-8
potassium cyanide

: 527-03-7, 93780-20-2
D-glycero-D-gulo-heptaric acid

: 6556-12-3
D-Glucuronic acid

: 526-97-6, 133-42-6, 488-33-5, 526-95-4, 576-36-3, 642-99-9, 1114-17-6, 3956-93-2, 6906-37-2, 7760-07-8, 13382-27-9, 20246-33-7, 20246-35-9, 20246-52-0, 20246-53-1, 21675-42-3, 22430-69-9, 24871-35-0, 28223-42-9, 28278-17-3, 51547-37-6
D-gluconic acid

Conditions

Conditions	Yield
With Ni-doped silica; ethanol at 120℃; under 36775.4 Torr; Hydrogenation;

: 6556-12-3
D-Glucuronic acid

: 469-44-3
2,3,4-trihydroxy-2-methyl-glutaric acid

Conditions

Conditions	Yield
With water; methyllithium; calcium carbonate

: 6556-12-3
D-Glucuronic acid

: 80-72-8
2,3-dihydroxy-2-cyclopenten-1-one

Conditions

Conditions	Yield
With sulfuric acid at 150℃;

: 6556-12-3
D-Glucuronic acid

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

Conditions

Conditions	Yield
untersucht wurde das Lactonisierungsgleichgewicht in wss. Loesungen vom pH 7 - 8.5;

: 6556-12-3
D-Glucuronic acid

: 106-49-0
p-toluidine

: 96933-51-6
1-p-toluidino-1-deoxy-β-D-glucopyranuronic acid

: 6556-12-3
D-Glucuronic acid

: 106-49-0
p-toluidine

: 109068-38-4
6-p-toluidino-D-lyxo-6-deoxy-[5]hexulosonic acid

D-Glucuronic acid Specification

The CAS register number of D-Glucuronic acid is 6556-12-3. It also can be called as Glucuronic acid and the IUPAC name about this chemical is (2S,3S,4S,5R)-3,4,5,6-tetrahydroxyoxane-2-carboxylic acid. The molecular formula about this chemical is C₆H₁₀O₇and the molecular weight is 194.14. It belongs to the following product categories, such as 13C & 2H Sugars; Biochemistry; Glucose; Sugars; Carbohydrates & Derivatives; Carbohydrate LibraryEnzyme Inhibitors by Enzyme; Glucuronidase, betaGlycobiology; InhibitorsAnalytical Enzymes; D to; Inhibitors and Substrates; Metabolic Libraries; Metabolomics; Related Products; β-Glucuronidase and so on.

Physical properties about D-Glucuronic acid are: (1)ACD/LogP: -2.88; (2)# of Rule of 5 Violations: 1; (3)ACD/BCF (pH 5.5): 1; (4)ACD/BCF (pH 7.4): 1; (5)ACD/KOC (pH 5.5): 1; (6)ACD/KOC (pH 7.4): 1; (7)#H bond acceptors: 7; (8)#H bond donors: 5; (9)#Freely Rotating Bonds: 5; (10)Polar Surface Area: 72.45Å²; (11)Index of Refraction: 1.685; (12)Molar Refractivity: 37.13 cm³; (13)Molar Volume: 97.6 cm³; (14)Polarizability: 14.72x10^-24cm³; (15)Surface Tension: 148.5 dyne/cm; (16)Enthalpy of Vaporization: 87.86 kJ/mol; (17)Boiling Point: 495.2 °C at 760 mmHg; (18)Vapour Pressure: 6.95E-12 mmHg at 25°C.

When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. When you are using it, wear suitable protective clothing, gloves and eye/face protection. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C(O)[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
(2)InChI: InChI=1/C6H10O7/c7-1-2(8)4(5(10)11)13-6(12)3(1)9/h1-4,6-9,12H,(H,10,11)/t1-,2-,3+,4-,6-/m0/s1
(3)InChIKey: AEMOLEFTQBMNLQ-WAXACMCWBB
(4)Std. InChI: InChI=1S/C6H10O7/c7-1-2(8)4(5(10)11)13-6(12)3(1)9/h1-4,6-9,12H,(H,10,11)/t1-,2-,3+,4-,6-/m0/s1
(5)Std. InChIKey: AEMOLEFTQBMNLQ-WAXACMCWSA-N

Product Name

D-Glucuronic acid

Synthetic route

D-Glucuronic acid Specification

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