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Dokumente

S7602

Sigma-Aldrich

Syringaldehyd

98%

Synonym(e):

4-Hydroxy-3,5-dimethoxy-benzaldehyd

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About This Item

Lineare Formel:
HOC6H2(OCH3)2CHO
CAS-Nummer:
134-96-3
Molekulargewicht:
182.17
Beilstein:
784514
EG-Nummer:
205-167-5
MDL-Nummer:
MFCD00006943
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24899757
NACRES:
NA.22

Qualitätsniveau

100

Assay

98%

bp

192-193 °C/14 mmHg (lit.)

mp (Schmelzpunkt)

110-113 °C (lit.)

SMILES String

COc1cc(C=O)cc(OC)c1O

InChI

1S/C9H10O4/c1-12-7-3-6(5-10)4-8(13-2)9(7)11/h3-5,11H,1-2H3

InChIKey

KCDXJAYRVLXPFO-UHFFFAOYSA-N

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Verwandte Kategorien

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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3,5-Dimethoxy-4-Hydroxyphenylessigsäure 97%

Sigma-Aldrich

631310

3,5-Dimethoxy-4-Hydroxyphenylessigsäure

n-Amyl 2-[3,5-dihydroxy-2-(1-nonanoyl)phenyl]acetate ≥98% (HPLC)

Sigma-Aldrich

A0987

n-Amyl 2-[3,5-dihydroxy-2-(1-nonanoyl)phenyl]acetate

4-Hydroxy-3,5-dimethoxybenzoic acid for synthesis

Sigma-Aldrich

8.22161

4-Hydroxy-3,5-dimethoxybenzoic acid

Syringaldazin 98%

Sigma-Aldrich

177539

Syringaldazin

4-Hydroxybenzaldehyd 98%

Sigma-Aldrich

144088

4-Hydroxybenzaldehyd

2,6-Dimethoxyphenol 99%

Sigma-Aldrich

D135550

2,6-Dimethoxyphenol

Cuimin Hu et al.
Bioresource technology, 100(20), 4843-4847 (2009-06-06)
Lignocellulosic biomass hydrolysis inevitably coproduces byproducts that may have various affects on downstream biotransformation. It is imperative to document the inhibitor tolerance ability of microbial strain in order to utilize biomass hydrolysate more effectively. To achieve better lipid production by
Palwinder Singh et al.
Journal of medicinal chemistry, 55(14), 6381-6390 (2012-06-28)
On the basis of structural analysis of dihydrofolate reductase (DHFR) (cocrystallized separately with NADPH, dihydrofolate and NADPH, trimethoprim), compounds 2 and 3 were optimized for inhibition of DHFR. Appreciable tumor growth inhibitory activities of compounds 2 and 3 over 60
Chia-Hsin Huang et al.
Journal of natural products, 75(8), 1465-1468 (2012-08-14)
The antihyperglycemic effect of syringaldehyde (1), purified from the stems of Hibiscus taiwanensis, was investigated in streptozotocin-induced diabetic rats (STZ-diabetic rats) showing type-1 like diabetes mellitus. Bolus intravenous injection of 1 showed antihyperglycemic activity in a dose-dependent manner in STZ-diabetic
Rogério S Pereira et al.
Journal of industrial microbiology & biotechnology, 38(1), 71-78 (2010-09-08)
The inhibitory action of acetic acid, ferulic acid, and syringaldehyde on metabolism of Candida guilliermondii yeast during xylose to xylitol bioconversion was evaluated. Assays were performed in buffered and nonbuffered semidefined medium containing xylose as main sugar (80.0 g/l), supplemented
Laura Mendoza et al.
Enzyme and microbial technology, 49(5), 478-484 (2011-11-25)
This paper presents the use of a membrane-integrated reactor system with recycling of laccase and mediator for azo dye decolorization. From initial screening of different laccases and mediators, Trametes versicolor laccase and syringaldehyde provided the best system for decolorization. Decolorization
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