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Merck

D134406

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

97%

Synonym(s):

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

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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
Assay:
97%
Form:
solid

Key Documents

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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

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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

D134406-5G: + D134406-25G: + D134406-BULK: + D134406-100G: + D134406-VAR: + D134406-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG4354
BCCG1783
BCCF0393
BCCD0300
0000086486

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Agrobacterium-mediated transformation of friable embryogenic calli and regeneration of transgenic cassava.
Bull SE, et al.
Nature Protocols, 4(12), 1845-1845 (2009)
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).
Tomoyuki Nabeshima et al.
Frontiers in plant science, 8, 1940-1940 (2017-12-19)
Chrysanthemum stunt viroid (CSVd) was inoculated into two chrysanthemum (
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
Haipeng Li et al.
Plant methods, 14, 50-50 (2018-07-07)
Genetically modified cotton accounts for 64% of the world's cotton growing area (22.3 million hectares). The genome sequencing of the diploid cotton progenitors Gossypium raimondii and Gossypium arboreum as well as the cultivated Gossypium hirsutum has provided a wealth of
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