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S7602

Sigma-Aldrich

Syringaldehyde

98%

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Synonym(s):
3,5-Dimethoxy-4-hydroxybenzaldehyde, 4-Hydroxy-3,5-dimethoxybenzaldehyde
Linear Formula:
HOC6H2(OCH3)2CHO
CAS Number:
Molecular Weight:
182.17
Beilstein:
784514
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

bp

192-193 °C/14 mmHg (lit.)

mp

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

InChI key

KCDXJAYRVLXPFO-UHFFFAOYSA-N

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This Item
W404926140392S6881
Syringaldehyde 98%

Sigma-Aldrich

S7602

Syringaldehyde

Syringaldehyde ≥98%, FG

Sigma-Aldrich

W404926

Syringaldehyde

Syringic acid ≥95% (HPLC)

Sigma-Aldrich

S6881

Syringic acid

bp

192-193 °C/14 mmHg (lit.)

bp

192-193 °C/14 mmHg (lit.)

bp

-

bp

-

mp

110-113 °C (lit.)

mp

110-113 °C (lit.)

mp

112-114 °C (lit.)

mp

205-209 °C (lit.)

Quality Level

100

Quality Level

400

Quality Level

100

Quality Level

100

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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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
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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
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The effect of lignin degradation products liberated during chemical hydrolysis of lignocellulosic materials on xylose-to-xylitol bioconversion by Candida guilliermondii FTI 20037 was studied. Two aromatic aldehydes (vanillin and syringaldehyde) were selected as model compounds. A two-level factorial design was employed

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