D133809
3,4-Dimethoxycinnamic acid, predominantly trans
99%
Synonym(s):
Caffeic acid dimethyl ether
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About This Item
Linear Formula:
(CH3O)2C6H3CH=CHCO2H
CAS Number:
Molecular Weight:
208.21
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
powder
mp
181-183 °C (lit.)
SMILES string
COc1ccc(\C=C\C(O)=O)cc1OC
InChI
1S/C11H12O4/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3-7H,1-2H3,(H,12,13)/b6-4+
InChI key
HJBWJAPEBGSQPR-GQCTYLIASA-N
Related Categories
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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[Chemical constituents of Veronicastrum sibiricum (L.) Pennell].
B Zhou et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 17(1), 35-36 (1992-01-01)
Tracy L Farrell et al.
Molecular nutrition & food research, 56(9), 1413-1423 (2012-08-07)
This study reports the 24 h human plasma pharmacokinetics of 3,4-dimethoxycinnamic acid (dimethoxycinnamic acid) after consumption of coffee, and the membrane transport characteristics of certain dimethoxycinnamic acid derivatives, as present in coffee. Eight healthy human volunteers consumed a low-polyphenol diet
Thiago Nogueira et al.
Electrophoresis, 28(19), 3570-3574 (2007-09-05)
A method based on the formation of pi-complexes with chlorogenate-like species was proposed for the determination of caffeine in regular (nondecaffeinated) and decaffeinated coffee. Both caffeate and 3,4-dimethoxycinnamate were able to transform caffeine--a neutral species in aqueous solutions--into an anionic
Maher M El-Domiaty et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 64(1-2), 11-19 (2009-03-28)
A new natural compound, named 6-O-(3",4"-dimethoxycinnamoyl) catalpol, was isolated from the defatted alcoholic extract of the flowering parts of Buddleja asiatica Lour. (family Scrophulariaceae). Other separated known compounds included steroids (beta-sitosterol, stigmasterol, stigmasterol-O-glucoside, beta-sitosterol-O-glucoside), iridoid glucosides (methyl catalpol, catalpol, aucubin)
A Sethuraman et al.
Applied microbiology and biotechnology, 52(5), 689-697 (1999-11-26)
Production of ligninolytic enzymes and degradation of 14C-ring labeled synthetic lignin by the white-rot fungus Cyathus stercoreus ATCC 36910 were determined under a variety of conditions. The highest mineralization rate for 14C dehydrogenative polymerizates (DHP; 38% 14CO2 after 30 days)
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