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T7407

Sigma-Aldrich

Trigalacturonic acid

≥90% (HPLC)

Synonym(s):

α-D-GalA-(1→4)-α-D-GalA-(1→4)-α-D-GalA, α-D-GalA-(1→4)-α-D-GalA-(1→4)-D-GalA

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About This Item

Empirical Formula (Hill Notation):
C18H26O19
CAS Number:
6037-45-2
Molecular Weight:
546.39
MDL number:
MFCD00079573
UNSPSC Code:
12352201
PubChem Substance ID:
24900452
NACRES:
NA.25

Quality Level

200

Assay

≥90% (HPLC)

form

powder

color

white

solubility

water: 50 mg/mL, clear, colorless

storage temp.

−20°C

SMILES string

OC(C=O)C(O)C(OC1OC(C(OC2OC(C(O)C(O)C2O)C(O)=O)C(O)C1O)C(O)=O)C(O)C(O)=O

InChI

1S/C18H26O19/c19-1-2(20)3(21)10(9(27)14(28)29)34-18-8(26)6(24)11(13(37-18)16(32)33)35-17-7(25)4(22)5(23)12(36-17)15(30)31/h1-13,17-18,20-27H,(H,28,29)(H,30,31)(H,32,33)

InChI key

FMNDXLWVYMQMHF-UHFFFAOYSA-N

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Other Notes

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Zhong Cheng et al.
Journal of microbiology and biotechnology, 26(6), 989-998 (2016-02-26)
Acidic endo-polygalacturonases are the major part of pectinase preparations and extensively applied in the clarification of fruits juice, vegetables extracts, and wines. However, most of the reported fungal endo-polygalacturonases are active and stable under narrow pH range and low temperatures.
Y Nakahara et al.
Carbohydrate research, 200, 363-375 (1990-04-25)
Syntheses of alpha-GalA-(1----4)-alpha-GalA-(1----4)-GalA, a proposed plant wound-hormone, and its stereoisomer beta-GalA-(1----4)-alpha-GalA-(1----4)-GalA are described. The key intermediates, tert-butyldiphenylsilyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-alpha-D-galactopyranosyl)-(1----4)-O-(6 -O- acetyl-2,3-di-O-benzyl-alpha-D-galactopyranosyl)-(1----4)-6-O-acetyl-2,3 -di-O- benzyl-beta-D-galactopyranoside and tert-butyldiphenylsilyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-beta-D-galactopyranosyl)-(1----4)-O-(6- O- acetyl-2,3-di-O-benzyl-alpha-D-galactopyranosyl)-(1----4)-6-O-acetyl-2,3 -di-O- benzyl-beta-D-galactopyranoside, were prepared by stereoselective alpha-glycosylation of tert-butyldiphenylsilyl 6-O-acetyl-2,3-di-O-benzyl-beta-D-galactopyranoside with O-(6-O-acetyl-2,3,4-tri-O-benzyl-alpha-D-galactopyranosyl)-(1----4)-6-O- acetyl-2,3-di-O-benzyl-D-galactopyranosyl
Judicaël Parisot et al.
Carbohydrate research, 337(16), 1427-1433 (2002-09-03)
A new exopolygalacturonate lyase (Pel) gene of the hyperthermophilic bacterium Thermotoga maritima was cloned and overexpressed in Escherichia coli cells. A 42 kDa monomeric Pel was shown to undergo N-terminal processing by cleavage at a putative site between alanine and
Simon J Charnock et al.
Proceedings of the National Academy of Sciences of the United States of America, 99(19), 12067-12072 (2002-09-11)
Enzyme-catalyzed beta-elimination of sugar uronic acids, exemplified by the degradation of plant cell wall pectins, plays an important role in a wide spectrum of biological processes ranging from the recycling of plant biomass through to pathogen virulence. The three-dimensional crystal
P Biely et al.
FEBS letters, 382(3), 249-255 (1996-03-18)
Endopolygalacturonases I and II (PGI and PGII) of Aspergillus niger and an exopolygalacturonase (ExoPG) of A. tubingensis were investigated to reveal the stereochemistry of their hydrolytic action. Reduced pentagalacturonic acid (pentaGalU-ol) and reduced trigalacturonic acid (triGalU-ol) were used as non-reducing
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