Skip to Content
Merck

D134406

3′,5′-Dimethoxy-4′-hydroxyacetophenone

97%

Synonym(s):

4′-Hydroxy-3′,5′-dimethoxyacetophenone, Acetosyringone

Sign In to View Organizational & Contract Pricing.

Select a Size

All Photos(2)

About This Item

Linear Formula:
HOC6H2(OCH3)2COCH3
CAS Number:
2478-38-8
Molecular Weight:
196.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893264
EC Number:
219-610-5
Beilstein/REAXYS Number:
1966119
MDL number:
MFCD00008748

Product Name

3′,5′-Dimethoxy-4′-hydroxyacetophenone, 97%

InChI

1S/C10H12O4/c1-6(11)7-4-8(13-2)10(12)9(5-7)14-3/h4-5,12H,1-3H3

InChI key

OJOBTAOGJIWAGB-UHFFFAOYSA-N

SMILES string

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

assay

97%

form

solid

mp

124-127 °C (lit.)

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

3′,5′-Dimethoxy-4′-hydroxyacetophenone has been used to activate the virulence (vir) genes of tumor-inducing (Ti) plasmid of Agrobacterium tumefaciens in Agrobacterium-mediated transformation (AMT) protocol.
3′,5′-Dimethoxy-4′-hydroxyacetophenone has been used to activate the virulence (vir) genes of tumor-inducing (Ti) plasmid of in Agrobacterium-mediated transformation (AMT) protocol.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000502513
0000502513
0000491806
0000491806
0000480490

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Agrobacterium-mediated transformation of friable embryogenic calli and regeneration of transgenic cassava.
Bull SE, et al.
Nature Protocols, 4(12), 1845-1845 (2009)
Tomoyuki Nabeshima et al.
Frontiers in plant science, 8, 1940-1940 (2017-12-19)
Chrysanthemum stunt viroid (CSVd) was inoculated into two chrysanthemum (
Jeongmin Choi et al.
Nature communications, 11(1), 2114-2114 (2020-05-02)
Most plants associate with beneficial arbuscular mycorrhizal (AM) fungi that facilitate soil nutrient acquisition. Prior to contact, partner recognition triggers reciprocal genetic remodelling to enable colonisation. The plant Dwarf14-Like (D14L) receptor conditions pre-symbiotic perception of AM fungi, and also detects
Brendon Conlan et al.
Plant, cell & environment, 42(4), 1287-1301 (2018-10-31)
The folding and assembly of Rubisco large and small subunits into L8 S8 holoenzyme in chloroplasts involves many auxiliary factors, including the chaperone BSD2. Here we identify apparent intermediary Rubisco-BSD2 assembly complexes in the model C3 plant tobacco. We show
Johana C Misas Villamil et al.
Nature communications, 10(1), 1576-1576 (2019-04-07)
Ustilago maydis is a biotrophic fungus causing corn smut disease in maize. The secreted effector protein Pit2 is an inhibitor of papain-like cysteine proteases (PLCPs) essential for virulence. Pit2 inhibitory function relies on a conserved 14 amino acids motif (PID14).
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service