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S7602

Syringaldehyde

Name: Syringaldehyde
Brand: ALDRICH

98%

Synonym(s):

3,5-Dimethoxy-4-hydroxybenzaldehyde, 4-Hydroxy-3,5-dimethoxybenzaldehyde

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About This Item

Linear Formula:

HOC₆H₂(OCH₃)₂CHO

CAS Number:

134-96-3

Molecular Weight:

182.17

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24899757

EC Number:

205-167-5

Beilstein/REAXYS Number:

784514

MDL number:

MFCD00006943

Assay:

98%

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Properties

Quality Level

100

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

Description

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pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Inhibitory action of toxic compounds present in lignocellulosic hydrolysates on xylose to xylitol bioconversion by Candida guilliermondii.

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

Effects of biomass hydrolysis by-products on oleaginous yeast Rhodosporidium toruloides.

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

Mechanism inspired development of rationally designed dihydrofolate reductase inhibitors as anticancer agents.

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

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Global Trade Item Number

SKU	GTIN
S7602-2G	04061832491172
S7602-5G	04061835282999
S7602-100G	04061832491158
S7602-25G	04061836960124