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SMB00103

Abietin

≥90% (LC/MS-ELSD)

Synonym(s):

Coniferin, Coniferoside, Coniferyl alcohol β-D-glucoside

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About This Item

Empirical Formula (Hill Notation):
C16H22O8
CAS Number:
531-29-3
Molecular Weight:
342.34
UNSPSC Code:
12352205
PubChem Substance ID:
329824781
NACRES:
NA.25

Key Documents

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Product Name

Abietin, ≥90% (LC/MS-ELSD)

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

assay

≥90% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

Related Categories

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
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
122228327V
12222818V
122228-18V

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Ping Huang et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 27(3), 173-175 (2004-07-27)
To study the major chemical constituents from the root tuber of Typhyonium flagelliforme. Compounds were separated and purified with silica gel column and preparative HPLC, and their structures were elucidated on the basis of spectroscopic evidence (UV, IR, MS, NMR
Yukiko Tsuji et al.
Journal of agricultural and food chemistry, 52(1), 131-134 (2004-01-08)
To examine the behavior of monolignol and monolignol glucosides in lignin biosynthesis, pentadeutero[9-D(2), 3-OCD(3)]coniferyl alcohol and pentadeutero[9-D(2), 3-OCD(3)]coniferin were synthesized and fed to growing Eucalyptus camaldulensis and Magnolia kobus. The differences in the incorporation patterns of these labeled precursors were
Han-wei Lin et al.
Biotechnology letters, 25(7), 521-525 (2003-07-29)
Linum flavum hairy roots were initiated from leaf discs using Agrobacterium rhizogenes strains LBA9402 and TR105 though two other strains, 15834 and A4, were relatively ineffective for induction. Significant variation in coniferin accumulation was observed between hairy root lines originating
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.
Vickram Beejmohun et al.
Phytochemistry, 68(22-24), 2744-2752 (2007-11-09)
[(13)C(2)]-Coniferin was provided to a flax (Linum usitatissimum L.) cell suspension to monitor subsequent dimerisation by MS and NMR. The label was mainly incorporated into a 8-8'-linked lignan, lariciresinol diglucoside, a 8-5'-linked neolignan, dehydrodiconiferyl alcohol glucoside and a diastereoisomeric mixture
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