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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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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

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
GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

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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Certificates of Analysis (COA)

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

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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
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
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
Christian Rolando et al.
Comptes rendus biologies, 327(9-10), 799-807 (2004-12-14)
Lignification was investigated in wild-type (WT) and in transgenic poplar plantlets with a reduced caffeic acid O-methyl-transferase (COMT) activity. Coniferin and syringin, deuterated at their methoxyl, were incorporated into the culture medium of microcuttings. The gas chromatography-mass spectrometry (GC-MS) analysis
L A Castle et al.
Journal of bacteriology, 174(5), 1478-1486 (1992-03-01)
Induction of Agrobacterium tumefaciens virulence genes by plant phenolic compounds is essential for successful T-DNA transfer to a host plant. In Douglas fir needles, the major virulence region inducer is the glycoside coniferin (J. W. Morris and R. O. Morris
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