D-(+)-Glucurono-3,6-lactone - CAS 32449-92-6
Catalog:
BB021291
Product Name:
D-(+)-Glucurono-3,6-lactone
CAS:
32449-92-6
Synonyms:
(2R)-2-[(2S,3R,4S)-3,4-dihydroxy-5-oxo-2-oxolanyl]-2-hydroxyacetaldehyde; D-Glucuronic acid, γ-lactone; D-Glucofuranurono-6,3-lactone; D-Glucuronic acid lactone; D-Glucurono-6,3-lactone; D-Glucurono-γ-lactone; D-Glucuronolactone; Dicurone; Glucoxy; Glucurolactone; Glucurone; Glucuronolactone; Guronsan; NSC 656
Ordering Information
Catalog
Size
Price
Stock
Quantity
BB021291
1 kg
$299
In stock
0
1
2
3
4
5
6
7
8
9
IUPAC Name: (2R)-2-[(2S,3R,4S)-3,4-dihydroxy-5-oxooxolan-2-yl]-2-hydroxyacetaldehyde
Description: D-(+)-Glucurono-3,6-lactone is used for treating canine hepatitis.
Molecular Weight: 176.12
Molecular Formula: C6H8O6
Canonical SMILES: C(=O)C(C1C(C(C(=O)O1)O)O)O
InChI: InChI=1S/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h1-5,8-10H/t2-,3+,4-,5+/m0/s1
InChI Key: UYUXSRADSPPKRZ-SKNVOMKLSA-N
Boiling Point: 403.5±28.0 °C at 760 mmHg
Melting Point: 172-175 °C (lit.)
Purity: ≥98%
Density: 1.8±0.1 g/cm3
Appearance: White to Off-white Solid
LogP: -2.80660
GHS Hazard Statement: H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement: P264, P270, P301+P312, P330, and P501
Signal Word: Warning
Publication Number Title Priority Date
CN-113512527-A Mesenchymal stem cell culture medium and application thereof 20210809
CN-113479880-A Preparation process of modified activated carbon 20210804
CN-113367248-A Feed, preparation method thereof and feeding method of laying hens 20210617
CN-113367249-A Additive and application thereof 20210617
CN-113265436-A Method for efficient biotransformation of anthraquinone products from traditional Chinese medicine sources by using streptomyces coeruleorubidus DM 20210607
PMID Publication Date Title Journal
31811891 20200130 d-Glucuronolactone attenuates para-xylene-induced defects in neuronal development and plasticity in Xenopus tectum in vivo Toxicology
22820017 20121101 In vivo role of aldehyde reductase Biochimica et biophysica acta
22928735 20120921 Glycosidase inhibition by all 10 stereoisomeric 2,5-dideoxy-2,5-iminohexitols prepared from the enantiomers of glucuronolactone The Journal of organic chemistry
22736508 20120723 Scalable syntheses of both enantiomers of DNJNAc and DGJNAc from glucuronolactone: the effect of N-alkylation on hexosaminidase inhibition Chemistry (Weinheim an der Bergstrasse, Germany)
22730801 20120501 [Energy drinks: an unknown risk] La Revue du praticien
Complexity: 202
Compound Is Canonicalized: Yes
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 4
Defined Bond Stereocenter Count: 0
Exact Mass: 176.03208797
Formal Charge: 0
Heavy Atom Count: 12
Hydrogen Bond Acceptor Count: 6
Hydrogen Bond Donor Count: 3
Isotope Atom Count: 0
Monoisotopic Mass: 176.03208797
Rotatable Bond Count: 2
Topological Polar Surface Area: 104 Å2
Undefined Atom Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
XLogP3: -1.8
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS