| Identification | Back Directory | [Name]
D-GALACTURONIC ACID | [CAS]
685-73-4 | [Synonyms]
galaturonate
GALACTURONATE
D-galaturonate
D-GALACTURONATE
D-GALACTURONIC ACID
GALACTURONIC ACID, D-
A-D-GALACTURONIC ACID
α-D-Galactouronic acid
D(+)-GALACTURONIC ACID
D-ALPHA-GALACTURONIC ACID
ALPHA-D-GALACTURONIC ACID
D-galactopyranuronic acid
aldehydo-D-galacturonicaci
aldehydo-D-galacturonic acid
D-GALACTURONIC ACID USP/EP/BP
D(+)-Galacturonic acid-1-hydrate
d-a-Galacturonic acid monohydrate
D-[UL-13C6]Galacturonic acid potassium salt | [EINECS(EC#)]
211-682-6 | [Molecular Formula]
C6H10O7 | [MDL Number]
MFCD00006618 | [MOL File]
685-73-4.mol | [Molecular Weight]
194.14 |
| Chemical Properties | Back Directory | [Appearance]
The α form melts with decomposition at 159–160C. Soluble in water, slightly soluble in hot alcohol; insoluble in ether | [Melting point ]
166°C | [Boiling point ]
250.56°C (rough estimate) | [density ]
1.4301 (rough estimate) | [refractive index ]
1.4455 (estimate) | [pka]
3.30±0.35(Predicted) | [LogP]
-1.490 (est) | [Uses]
Biochemical research | [EPA Substance Registry System]
D-Galacturonic acid (685-73-4) |
| Hazard Information | Back Directory | [Chemical Properties]
The α form melts with decomposition at 159–160C. Soluble in water, slightly soluble in hot alcohol; insoluble in ether | [Definition]
ChEBI: The pyranose form of D-galacturonic acid | [Description]
D-Galacturonic acid is a sugar acid, an oxidized form of Dgalactose. It is the main component of pectin, in which it exists as the polymer polygalacturonic acid. It has an aldehyde group at C1 and a carboxylic acid group at C6. Other oxidized forms of D-galactose are D-galactonic acid (carboxylic group at C1) and meso-galactaric acid (mucic acid) (carboxylic groups at C1 and C6). It is also a uronic acid or hexuronic acid. Naturally occurring uronic acids are D-glucuronic acid, D-galacturonic acid, L-iduronic acid and D-mannuronic acid. | [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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