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D4288

Digalacturonic acid

≥85% (HPLC)

Sinónimos:

α-D-GalA-(1→4)-D-GalA

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Fórmula empírica (notación de Hill):
C12H18O13
Número CAS:
Peso molecular:
370.26
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
MDL number:
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biological source

synthetic (organic)

Quality Level

assay

≥85% (HPLC)

form

powder

color

white to off-white

solubility

water: 50 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

SMILES string

OC(C=O)C(O)C(OC1OC(C(O)C(O)C1O)C(O)=O)C(O)C(O)=O

InChI

1S/C12H18O13/c13-1-2(14)3(15)8(7(19)10(20)21)24-12-6(18)4(16)5(17)9(25-12)11(22)23/h1-9,12,14-19H,(H,20,21)(H,22,23)

InChI key

SYBQLSSECRIKMJ-UHFFFAOYSA-N

Application

Digalacturonic acid (DGA), derived in vivo from pectin catabolism, is used for the co-crystallization of enzymes such as proteinase K. It is used in galacturonic acid metabolism research as a substrate to identify, differentiate and characterized endo- and exopolygalacturonase(s) and gluconase(s). DGA is used to study the transport of oligogalacturonides by systems such as the TogMNAB ABC transporter.

Other Notes

To gain a comprehensive understanding of our extensive range of Disaccharides for your research, we encourage you to visit our Carbohydrates Category page.

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Este artículo
T7407G9662C8286
assay

≥85% (HPLC)

assay

≥90% (HPLC)

assay

≥90%

assay

≥85% (HPLC)

biological source

synthetic (organic)

biological source

-

biological source

synthetic

biological source

synthetic (organic)

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

solubility

water: 50 mg/mL, clear, colorless to faintly yellow

solubility

water: 50 mg/mL, clear, colorless

solubility

-

solubility

water: 25 mg/mL, clear, colorless to faintly yellow

form

powder

form

powder

form

powder or solid

form

powder

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C


Clase de almacenamiento

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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Leonel M Ortega et al.
Journal of basic microbiology, 54 Suppl 1, S170-S177 (2014-01-10)
Since enzymatic degradation is a mechanism or component of the aggressiveness of a pathogen, enzymatic activities from a Fusarium graminearum isolate obtained from infected wheat spikes of Argentina Pampa region were studied in order to understand the disease progression, tending
D Wade Abbott et al.
Journal of molecular biology, 369(3), 759-770 (2007-04-25)
The process of pectin depolymerization by pectate lyases and glycoside hydrolases produced by pectinolytic organisms, particularly the phytopathogens from the genus Erwinia, is reasonably well understood. Indeed each extracellular and intracellular catabolic stage has been identified using either genetic, bioinformatic
C Gouvion et al.
Carbohydrate research, 261(2), 187-202 (1994-08-17)
The solution conformation of digalacturonic acid and its sodium salt have been analyzed using nuclear magnetic resonance data and molecular mechanics calculations. The flexibility around the glycosidic linkage was characterized by calculation of the relaxed (phi, psi) potential surfaces for



Número de artículo de comercio global

SKUGTIN
D4288-100MG04061832961552
D4288-25MG04061832961576
D4288-10MG04061833564257

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