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Key Documents

D134406

Sigma-Aldrich

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:
Molecular Weight:
196.20
Beilstein:
1966119
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

124-127 °C (lit.)

SMILES string

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

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

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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

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 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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)
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