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223735

Sigma-Aldrich

Coniferyl alcohol

98%

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Synonym(s):
3-(4-Hydroxy-3-methoxyphenyl)-2-propen-1-ol, 4-Hydroxy-3-methoxycinnamyl alcohol
Linear Formula:
HOC6H3(OCH3)CH=CHCH2OH
CAS Number:
Molecular Weight:
180.20
Beilstein:
2048961
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

solid

bp

163-165 °C/3 mmHg (lit.)

mp

75-80 °C (lit.)

solubility

alcohol: moderately soluble(lit.)
diethyl ether: freely soluble(lit.)
water: insoluble (almost)

storage temp.

−20°C

SMILES string

COc1cc(\C=C\CO)ccc1O

InChI

1S/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3/b3-2+

InChI key

JMFRWRFFLBVWSI-NSCUHMNNSA-N

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This Item
240532G104641402
Coniferyl alcohol 98%

Sigma-Aldrich

223735

Coniferyl alcohol

Allyl alcohol ≥99%

Sigma-Aldrich

240532

Allyl alcohol

[6]-Gingerol ≥98% (HPLC)

Sigma-Aldrich

G1046

[6]-Gingerol

Coniferyl alcohol analytical standard

Supelco

41402

Coniferyl alcohol

form

solid

form

liquid

form

-

form

-

bp

163-165 °C/3 mmHg (lit.)

bp

96-98 °C (lit.)

bp

-

bp

163-165 °C/3 mmHg (lit.)

mp

75-80 °C (lit.)

mp

−129 °C (lit.)

mp

-

mp

75-80 °C (lit.)

solubility

alcohol: moderately soluble(lit.), diethyl ether: freely soluble(lit.), water: insoluble (almost)

solubility

alcohol: miscible(lit.), chloroform: miscible(lit.), diethyl ether: miscible(lit.), water: miscible(lit.)

solubility

methanol: 1 mg/mL, clear, colorless

solubility

-

storage temp.

−20°C

storage temp.

-

storage temp.

−20°C

storage temp.

−20°C

General description

Coniferyl alcohol is one of the preferred substrate of the eucalpytus globus enzyme.

Application

Coniferyl alcohol was used as a fungal growth inhibitor.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Stefanie König et al.
The New phytologist, 202(3), 823-837 (2014-02-04)
Verticillium longisporum is a soil-borne vascular pathogen causing economic loss in rape. Using the model plant Arabidopsis this study analyzed metabolic changes upon fungal infection in order to identify possible defense strategies of Brassicaceae against this fungus. Metabolite fingerprinting identified
José Renán García et al.
Plant cell reports, 33(8), 1263-1274 (2014-04-17)
The gene coding for F5H from Eucalyptus globulus was cloned and used to transform an f5h -mutant of Arabidopsis thaliana , which was complemented, thus verifying the identity of the cloned gene. Coniferaldehyde 5-hydroxylase (F5H; EC 1.14.13) is a cytochrome
Paula Oyarce et al.
Nature plants, 5(2), 225-237 (2019-01-30)
Lignin is the main cause of lignocellulosic biomass recalcitrance to industrial enzymatic hydrolysis. By partially replacing the traditional lignin monomers by alternative ones, lignin extractability can be enhanced. To design a lignin that is easier to degrade under alkaline conditions
Guilhem Reyt et al.
Nature communications, 12(1), 2320-2320 (2021-04-21)
Lignin is a complex polymer deposited in the cell wall of specialised plant cells, where it provides essential cellular functions. Plants coordinate timing, location, abundance and composition of lignin deposition in response to endogenous and exogenous cues. In roots, a
Alif Meem Nurani et al.
Plant & cell physiology, 61(2), 255-264 (2020-01-11)
Stem cells undergo cell division and differentiation to ensure organized tissue development. Because plant cells are immobile, plant stem cells ought to decide their cell fate prior to differentiation, to locate specialized cells in the correct position. In this study

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