Structure of D Glucuronic acid CAS 6556 12 370021 34 0 - D-Glucuronic acid CAS 6556-12-3(70021-34-0)

Iden­ti­fi­ca­tion

CAS Number

6556-12-3(70021-34-0)

Name

D-Glu­curon­ic acid

Syn­onyms

α-D-Glu­­copy­­ra­nuron­ic acid [ACD/​Index Name] [ACD/IUPAC Name]
6556-12-3 [RN]
70021-34-0 [RN]
Acide α-D-glu­­copy­­ra­nuronique [French] [ACD/IUPAC Name]
D-Glu­­copy­­ra­nuron­ic acid [ACD/​Index Name] [ACD/IUPAC Name]
D-Glu­curon­ic acid [ACD/​Index Name] [ACD/IUPAC Name]
α-D-Glu­­copy­­ra­nuron­säure [Ger­man] [ACD/IUPAC Name]
α-D-glu­curon­ic acid
Glu­cosiduronate
Glu­cosiduron­ic acid
(2S,3S,4S,5R,6S)-3,4,5,6-tetrahydroxy-2-tetrahydropyrancarboxylic acid
(2S,3S,4S,5R,6S)-3,4,5,6-tetrahydroxyoxane-2-carboxylic acid
(2S,3S,4S,5R,6S)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylic acid
(2S,3S,4S,5R,6S)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylic acid ; α-D-glu­­copy­­ra­nuron­ic acid
(2S,3S,4S,5R,6S)-3,4,5,6-tetrahydroxytetrahydropyran-2-carboxylic acid
03/12/6556
106499-29-0 [RN]
1285548 [Beil­stein]
CHEBI:42717
D-(+)-glucuronate
D-(+)-glucuronic acid
D-Glu­curonate [ACD/IUPAC Name]
GCU
glc
GlcAa
GlcAal­pha
glu­curonate [Wiki]
Glu­curon­ic acid [Wiki]
α-D-Glu­cose
α-D-GLU­CURON­IC ACID
β-D-glu­curon­ic acid
δ-glu­curonate
葡糖醛酸 [Chi­nese]

SMILES

[C@@H]1([C@@H]([C@H](O[C@@H]([C@@H]1O)O)C(=O)O)O)O

Std­InChI

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

Std­InChIKey

AEMOLEFT­QBMN­LQWAX­ACM­CWSA-N

Mol­e­c­u­lar Formula

C6H10O7

Mol­e­c­u­lar Weight

194.139

EINECS

229-486-4

Beil­stein Reg­istry Number

1727083

MDL Number

MFCD00077778 

Prop­er­ties

Appear­ance

White crys­talline powder

Safe­ty Data

Per­son­al Pro­tec­tive Equipment

Eye­shieldsGlovestype N95 (US)type P1 (EN143) res­pi­ra­tor filter

RIDADR 

NONH for all modes of transport 

WGK Germany

3

RTECS 

LZ8836600

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our D-Glu­curon­ic acid CAS 6556-12-3(70021-34-0)

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

Puri­ty

98% min

Spe­cif­ic Opti­cal Rotation

+11.7~+36.3°

Heavy Met­als

≤1 ppm

Chlo­ride

≤10 ppm 

Loss on Drying 

≤0.8%

Residue on Ignition

≤1 ppm 

Sul­fate

≤10 ppm 

Arsenic

≤1 ppm

Nick­el

≤0.5 ppm

Iron

≤1 ppm

Microor­gan­ism Total count

Not Detect­ed

Yeast/​Mould count

Not Detect­ed

Escherichia coli

Not Detect­ed

Stor­age

Under room tem­per­a­ture away from light

Known Appli­ca­tion

D-Glu­curon­ic acid is wide­ly dis­trib­uted in the plant and ani­mal king­doms. D-Glu­curon­ic acid usu­al­ly occurs form as a gly­co­sidic com­bi­na­tion with phe­nols, alco­hols. Such glu­curonides form in the liv­er to detox­i­fy poi­so­nous hydrox­­yl-con­­tain­ing sub­stances. The glu­curonides present in nor­mal urine are those of phe­nol, cresol, and indoxyl. After the inges­tion of poi­sons such as mor­phine, chlo­ral hydrate, cam­phor, or tur­pen­tine, glu­curonides formed with the poi­son or its hydrox­y­lat­ed deriv­a­tives appear in the urine. 

This prod­uct is devel­oped by our R&D com­pa­ny Ulcho Bio­chem­i­cal Ltd(http://​www​.ulcho​.com/), and here is the cor­re­spond­ing linkhttp://​www​.ulcho​.com/​d​-​g​l​u​c​u​r​o​n​i​c​-​a​c​i​d​-​c​a​s​-​6​5​5​6​-​1​2​-​3​7​0​0​2​1​-​3​4​-0/

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