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SMB00103

Sigma-Aldrich

Abietin

≥90% (LC/MS-ELSD)

Synonym(s):

Coniferin, Coniferoside, Coniferyl alcohol β-D-glucoside

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£278.00

About This Item

Empirical Formula (Hill Notation):
C16H22O8
CAS Number:
Molecular Weight:
342.34
UNSPSC Code:
12352205
PubChem Substance ID:
NACRES:
NA.25

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Assay

≥90% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

COc1cc(C\C=C\O)ccc1O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O

InChI

1S/C16H22O8/c1-22-11-7-9(3-2-6-17)4-5-10(11)23-16-15(21)14(20)13(19)12(8-18)24-16/h2,4-7,12-21H,3,8H2,1H3/b6-2+/t12-,13-,14+,15-,16-/m1/s1

InChI key

XQIJIPVRXMWYLN-GLIXSRQJSA-N

General description

Abietin, also known as Coniferin, is a glucoside of coniferyl alcohol that is also found in the water root extract of Angelica archangelica subsp. litoralis.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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K Ito et al.
Bioscience, biotechnology, and biochemistry, 64(3), 584-587 (2000-05-10)
The fraction containing glycosidic components was separated from flue-cured tobacco (Nicotiana tabacum L.) leaves by a facile method. Some components of the fraction were isolated and elucidated to be syringin, coniferin, cichoriin, benzyl-beta-D-glucoside, Blumenol A-beta-D-glucoside, and 5,6-epoxy-5,6-dihydro-3-hydroxy-beta-ionyl-beta-D-glucoside. Syringin and coniferin
Mei-hua Han et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 32(17), 1755-1759 (2007-11-13)
To study the bioactive constituents of the fresh rhizome of Pinellia ternata, and provide the scientific basis for quality control. Various chromatographic techniques were used to separate and purify the chemical constituents, and their chemical structures were determined on the
A L Samuels et al.
Planta, 216(1), 72-82 (2002-11-14)
The objectives of this study were to define cell structure during pine secondary xylem development and to integrate this information with current knowledge of the biochemistry and physiology of secondary cell wall biosynthesis in gymnosperms. Lodgepole pine (Pinus contorta var.
Yukiko Tsuji et al.
Planta, 222(1), 58-69 (2005-06-30)
To gain insight into the behavior of monolignol glucoside in Ginkgo biloba L., we examined glucosides potentially involved in lignin biosynthetic pathway. Coniferin (coniferyl alcohol 4O-beta-D-glucoside) is a strong candidate for the storage form of monolignol. Coniferaldehyde glucoside may also
E Yamamoto et al.
Plant physiology, 94, 209-213 (1990-01-01)
American beech (Fagus grandifolia Ehrh) bark exclusively accumulates cis-monolignols and their glucosidic conjugates; no evidence for the accumulation of trans-monolignols has been found. The glucosyltransferase from this source exhibits a very unusual substrate specificity for cis, and not trans, monolignols.

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