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Catalogue Number
BN-O1720
Analysis Method
HPLC,NMR,MS
Specification
98%(HPLC)
Storage
-20℃
Molecular Weight
208.2
Appearance
Powder
Botanical Source
This product is isolated and purified from the herbs of Sarcandra glabra
Structure Type
Saccharides
Category
Standards;Natural Pytochemical;API
SMILES
CCOC1C(C(C(C(O1)CO)O)O)O
Synonyms
D-Glucopyranoside, ethyl/Ethyl D-glucopyranoside
IUPAC Name
(3R,4S,5S,6R)-2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol
Applications
Density
1.4±0.1 g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
192.7±27.9 °C
Boiling Point
395.1±42.0 °C at 760 mmHg
Melting Point
InChl
InChI=1S/C8H16O6/c1-2-13-8-7(12)6(11)5(10)4(3-9)14-8/h4-12H,2-3H2,1H3/t4-,5-,6+,7-,8-/m1/s1
InChl Key
WYUFTYLVLQZQNH-JAJWTYFOSA-N
WGK Germany
RID/ADR
HS Code Reference
2933990000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:3198-49-0) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
14978530
Metabonomic screening of human urine samples using 1H NMR spectroscopy has revealed the presence of signals resulting from the excretion of ethyl glucoside. Experiments in volunteers have demonstrated that this ethyl glucoside results from dietary exposure to the compound, which is present in beverages such as rice wine and sake, rather than representing a new route for the metabolism of ethanol by humans. The limited studies undertaken in volunteers indicate that ethyl glucoside has a longer biological half life than ethanol itself. The potential problems associated with using this glucoside metabolite as a marker of ethanol consumption are considered.
Ethyl glucoside in human urine following dietary exposure: detection by 1H NMR spectroscopy as a result of metabonomic screening of humans.
Teague C1, Holmes E, Maibaum E, Nicholson J, Tang H, Chan Q, Elliott P, Stamler J, Ueshima H, Zhou B, Wilson I.
2004 Mar
