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PHL80007

trans-Sinapic acid

phyproof® Reference Substance

Synonym(s):

trans-4-Hydroxy-3,5-dimethoxy-cinnamic acid, trans-Sinapinic acid

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25 G
¥226.99
100 G
¥686.80

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25 G
¥226.99
100 G
¥686.80

About This Item

Empirical Formula (Hill Notation):
C11H12O5
CAS Number:
7362-37-0
Molecular Weight:
224.21
MDL number:
MFCD00004401
UNSPSC Code:
41116107
NACRES:
NA.24

¥226.99

Please contact Customer Service for Availability
Request a Bulk Order

grade

primary reference standard

product line

phyproof® Reference Substance

Assay

≥95.0% (HPLC)

manufacturer/tradename

PhytoLab

SMILES string

COc1cc(\C=C\C(O)=O)cc(OC)c1O

InChI

1S/C11H12O5/c1-15-8-5-7(3-4-10(12)13)6-9(16-2)11(8)14/h3-6,14H,1-2H3,(H,12,13)/b4-3+

InChI key

PCMORTLOPMLEFB-ONEGZZNKSA-N

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Show Differences

1 of 4

This Item
125881100900411973
3-溴苯胺 98%

180025

3-溴苯胺

2,5-二溴苯胺 98%

125881

2,5-二溴苯胺

4-溴苯胺 97%

100900

4-溴苯胺

1,2,3-三氯-5-硝基苯 96%

411973

1,2,3-三氯-5-硝基苯

assay

98%

assay

98%

assay

97%

assay

96%

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

-

refractive index

n20/D 1.625 (lit.)

refractive index

-

refractive index

-

refractive index

-

mp

15-18 °C (lit.)

mp

51-53 °C (lit.)

mp

56-62 °C (lit.)

mp

68-71 °C (lit.)

density

1.58 g/mL at 25 °C (lit.)

density

-

density

-

density

-

form

liquid

form

solid

form

solid

form

-

General description

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

Other Notes

This compound is commonly found in plants of the genus: carum cinnamomum melissa salvia thymus zingiber

Legal Information

phyproof is a registered trademark of PhytoLab GmbH & Co. KG

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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    Certificates of Analysis (COA)

    Lot/Batch Number
    247970
    99776
    110145950

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    Hye Jin Kim et al.
    Phytochemical analysis : PCA, 22(3), 258-262 (2010-10-29)
    Direct analysis in real time (DART) ion source is a powerful ionising technique for the quick and easy detection of various organic molecules without any sample preparation steps, but the lack of quantitation capacity limits its extensive use in the
    Ju-Xian Song et al.
    Phytotherapy research : PTR, 25(3), 435-443 (2010-08-27)
    Aggregated beta-amyloid (Aβ) and elevated plasma levels of homocysteine have been implicated as critical factors in the pathogenesis of Alzheimer's disease. The neuroprotective effects and possible mechanism of four structurally similar dibenzocyclooctadiene lignans (namely schisandrin, schisantherin A, schisandrin B and
    Meng-Shiou Lee et al.
    Molecules (Basel, Switzerland), 18(1), 354-372 (2012-12-29)
    Glutamate-induced excitotoxicity has been implicated in a variety of neuronal degenerative disorders. In the present study, we investigated the possible neuroprotective effects of schizandrin against apoptosis of primary cultured rat cortical cells induced by glutamate. Glutamate (10 μM) administered for
    Di Hu et al.
    Oxidative medicine and cellular longevity, 2012, 721721-721721 (2012-07-26)
    In the present study, we examined the effect of schisandrin (SCH) of Schisandra chinensis on the amyloid-beta(1-42)- (Aβ(1-42)-) induced memory impairment in mice and elucidated the possible antioxidative mechanism. Mice were intracerebroventricular (i.c.v.) injected with the aggregated Aβ(1-42) and then
    Elina Hakala et al.
    The Journal of antibiotics, 68(10), 609-614 (2015-05-07)
    Lignans from Schisandra chinensis berries show various pharmacological activities, of which their antioxidative and cytoprotective properties are among the most studied ones. Here, the first report on antibacterial properties of six dibenzocyclooctadiene lignans found in Schisandra spp. is presented. The
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