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1-(3,4-Dimethoxyphenyl)propane-1,2-diol
1-(3,4-Dimethoxyphenyl)propane-1,2-diol
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 1-(3,4-Dimethoxyphenyl)propane-1,2-diol
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CAS No.: 20133-19-1
Catalog No.: CFN98017
Molecular Formula: C11H16O4
Molecular Weight: 212.2 g/mol
Purity: >=98%
Type of Compound: Phenylpropanoids
Physical Desc.: Powder
Source: The herbs of Chloranthus elatior
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
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Description: Standard reference
1-(3,4-Dimethoxyphenyl)propane-1,2-diol Description
Source: The herbs of Chloranthus elatior
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

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Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.7125 mL 23.5627 mL 47.1254 mL 94.2507 mL 117.8134 mL
5 mM 0.9425 mL 4.7125 mL 9.4251 mL 18.8501 mL 23.5627 mL
10 mM 0.4713 mL 2.3563 mL 4.7125 mL 9.4251 mL 11.7813 mL
50 mM 0.0943 mL 0.4713 mL 0.9425 mL 1.885 mL 2.3563 mL
100 mM 0.0471 mL 0.2356 mL 0.4713 mL 0.9425 mL 1.1781 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Journal of Molecular Catalysis B: Enzymatic.2000 Feb;8(4-6):213–219.
Laccase-catalyzed oxidation of 1-(3,4-dimethoxyphenyl)-1-propene using ABTS as mediator.[Reference: WebLink]

METHODS AND RESULTS:
The fungal laccases catalyzed oxidation of 1-(3,4-dimethoxyphenyl)-1-propene (2) with dioxygen in acetate buffer (pH 4.5) producing 1-(3,4-Dimethoxyphenyl)propane-1,2-diol (4) and its 1-O-acetyl and 2-O-acetyl derivatives 5 and 6, and 3,4-dimethoxybenzaldehyde (7). However, in phosphate buffer (pH 5.9), the same reaction produced only 1-(3,4-Dimethoxyphenyl)propane-1,2-diol and 7.
CONCLUSIONS:
When 1-(3,4-Dimethoxyphenyl)propane-1,2-diol was treated in the same fashion in the phosphate buffer, it was converted into 7 with more than 95 mol% yield.
CFN91026Methyl Kakuol70342-29-9208.21C11H12O4
CFN99493Junipediol B144881-19-6196.2 C10H12O4
CFN96122Junipediol B 8-O-glucoside188894-19-1358.3C16H22O9
CFN95643Guaiacylglycerol 8-O-beta-D-glucopyranoside109280-40-2376.4C16H24O10
CFN95644(2R)-3-Hydroxy-2-[4-(3-hydroxypropyl)-2- methoxyphenoxy]propyl beta-D-glucopyranoside198817-97-9418.4C19H30O10
CFN95645(2S)-3-Hydroxy-2-[4-(3-hydroxypropyl)-2- methoxyphenoxy]propyl beta-D-glucopyranoside198817-98-0418.4C19H30O10
CFN96100threo-1-(4-Hydroxy-3-methoxyphenyl)propane-1,2-diol848031-94-7198.2C10H14O4
CFN96099erythro-1-(4-Hydroxy-3-methoxyphenyl)propane-1,2-diol1280602-81-4198.2C10H14O4
CFN98327threo-Guaiacylglycerol27391-16-8214.2 C10H14O5
CFN98619erythro-Guaiacylglycerol38916-91-5214.2 C10H14O5
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