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ALPHA-D-GALACTURONIC ACID HYDRATE

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ALPHA-D-GALACTURONIC ACID HYDRATE Basic information

Product Name:
ALPHA-D-GALACTURONIC ACID HYDRATE
Synonyms:
  • ALPHA-D-GALACTURONIC
  • alpha-D-Galacturonic Acid 
  • D(+)-Galacturonic acid monohydrate,99%
  • D-Galacturonic acid hydrate
  • D-(+)-Galacturonic acid Monohydrat
  • D-Galacturonic acid Monohyarate
  • D-(+)-Galacturonic acid Monohydrate >=97.0%
  • (2S,3R,4S,5R)
CAS:
91510-62-2
MF:
C6H12O8
MW:
212.15
EINECS:
211-682-6
Product Categories:
  • Carbohydrates & Derivatives
  • Sugar Acids
  • Sugars
  • Carbohydrate Synthesis
  • Monosaccharides
  • Specialty Synthesis
  • Biochemistry
  • Galactose
Mol File:
91510-62-2.mol
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ALPHA-D-GALACTURONIC ACID HYDRATE Chemical Properties

Melting point:
156-159℃
alpha 
+51.7°(23℃/D, c=1, H2O)
refractive index 
52.5 ° (C=10, H2O)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
DMSO (Slightly, Sonicated), Methanol (Slightly), Water (Slightly)
form 
Powder
color 
White to Off-white
optical activity
[α]20/D +53±2°, 5 hr, c = 10% in H2O
Water Solubility 
Soluble in water
Merck 
14,4337
BRN 
1727087
CAS DataBase Reference
91510-62-2(CAS DataBase Reference)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
TSCA 
Yes
HS Code 
29329990
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ALPHA-D-GALACTURONIC ACID HYDRATE Usage And Synthesis

Chemical Properties

white to light beige fine powder

Uses

D-(+)-Galacturonic acid monohydrate is a chemical used in the synthesis of N-(D-galacturonoyl) amino acids and dipeptides.

Uses

ALPHA-D-GALACTURONIC ACID HYDRATE is highly purified product form Pectine.It is used in the synthesis of N-(D-galacturonoyl) amino acids and dipeptides.

Purification Methods

Crystallisation of the acid from 95% EtOH and drying it in a vacuum desiccator (12mm) over P2O5 gives the monohydrate mixture of and anomers (mostly -) as white micro needles, which sinter at ~100-111o and melt at 159-160o, [] D 20 +107o (initial, c 4 in H2O mutarotating to +51o). [Link & Sell Biochemical Preparations 3 74, 78 1953, Beilstein 3 IV 2000.] The -anomer is obtained by warming the -anomer in EtOH, AcOH or EtOAc and has m 1 6 0o (165o, sinters at 1 4 0o), [] D 20 +27o (initial, c 2 in H2O mutarotating to +55.3o in 24hours). The sodium salt [14984-39-5] M 216.1 has [] D 20 +27o (c 10 in H2O after 5hours). The phenylhydrazone has m 141o(from MeOH). [Ehrlich & Schubert Chem Ber 62 1974, 2014 1929, Anderson & King J Chem Soc 5333 1961, Beilstein 3 IV 2001.]

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