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SMB00103

Sigma-Aldrich

Abietin

≥90% (LC/MS-ELSD)

Synonyma:

Coniferin, Coniferoside, Coniferyl alcohol β-D-glucoside

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About This Item

Empirický vzorec (Hillův zápis):
C16H22O8
Číslo CAS:
531-29-3
Molekulová hmotnost:
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

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Vyberte jednu z posledních verzí:

Osvědčení o analýze (COA)

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

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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
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
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
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