JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.

This is a demo store. No orders will be fulfilled.

Account

Settings

Language

྾

Home
Chemistry & Biochemicals
Building Blocks
Organic Building Blocks
3',4'-Dimethoxyacetophenone - >98.0%(GC), high purity , CAS No.1131-62-0

Skip to the end of the images gallery

Skip to the beginning of the images gallery

3',4'-Dimethoxyacetophenone - >98.0%(GC), high purity , CAS No.1131-62-0

2 Citations

COA

Grade & Purity:

≥98%(GC)

Cas Number: 1131-62-0
Molecular Weight: 180.2
Beilstein Registry Number: 781213
EC Number: 214-468-0
MDL number: MFCD00008737
PubChem CID: 14328
PubChem SID: 504752552

In stock

Item Number

D154231

Grouped product items
SKU	Size	Availability	Price
D154231-5g	5g	3	$12.90
D154231-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$19.90
D154231-25g	25g	10	$37.90
D154231-100g	100g	9	$115.90
D154231-250g	250g	3	$222.90
D154231-500g	500g	2	$342.90

View related series

ketone (798) Non heterocyclic block (8163)

Basic Description

Synonyms	3',4'-Dimethoxyacetophenone, >=98% \| 4'-Hydroxy-3'-methoxyacetophenone, methyl ether \| AI3-11163 \| AQ-917/40710349 \| 3,4-Dimethoxyphenyl methyl ketone \| GF-0115 \| 3,4-dimethoxy acetophenone \| Acetophenone, 3',4'-dimethoxy- \| D1878 \| SY015105 \| 3',4'-Dimet
Specifications & Purity	≥98%(GC)
Storage Temp	Protected from light,Room temperature
Shipped In	Normal
Product Description	Product Application： 3',4'-Dimethoxyacetophenone is used as Catalytic agent; Petrochemical additive. It is also used in agrochemical, pharmaceutical and dyestuff field.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organooxygen compounds
    - Subclass Carbonyl compounds
      - Level5 Ketones
        Level6 Aryl ketones
        Level7 Phenylketones
        Level8 Alkyl-phenylketones

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organooxygen compounds
Subclass	Carbonyl compounds
Intermediate Tree Nodes	Ketones - Aryl ketones - Phenylketones
Direct Parent	Alkyl-phenylketones
Alternative Parents	Dimethoxybenzenes Acetophenones Phenoxy compounds Benzoyl derivatives Aryl alkyl ketones Anisoles Alkyl aryl ethers Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Alkyl-phenylketone - O-dimethoxybenzene - Dimethoxybenzene - Acetophenone - Phenoxy compound - Methoxybenzene - Aryl alkyl ketone - Anisole - Phenol ether - Benzoyl - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Ether - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
External Descriptors	dimethoxybenzene - acetophenones
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

TYR Tclin Tyrosinase (717 Activities)

Discover Target: TYR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504752552
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504752552
IUPAC Name	1-(3,4-dimethoxyphenyl)ethanone
INCHI	InChI=1S/C10H12O3/c1-7(11)8-4-5-9(12-2)10(6-8)13-3/h4-6H,1-3H3
InChIKey	IQZLUWLMQNGTIW-UHFFFAOYSA-N
Smiles	CC(=O)C1=CC(=C(C=C1)OC)OC
Isomeric SMILES	CC(=O)C1=CC(=C(C=C1)OC)OC
WGK Germany	3
Molecular Weight	180.2
Beilstein	781213
Reaxy-Rn	781213
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=781213&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

15 results found

Lot Number	Certificate Type	Date	Item
K2020230	Certificate of Analysis	Sep 09, 2024	D154231
K2020229	Certificate of Analysis	Sep 09, 2024	D154231
G2410165	Certificate of Analysis	Apr 27, 2024	D154231
C2521418	Certificate of Analysis	Apr 27, 2024	D154231
C2521419	Certificate of Analysis	Apr 27, 2024	D154231
C2521420	Certificate of Analysis	Apr 27, 2024	D154231
J1808055	Certificate of Analysis	Aug 08, 2022	D154231
B2210429	Certificate of Analysis	Dec 30, 2021	D154231
B2210279	Certificate of Analysis	Dec 30, 2021	D154231
B2210270	Certificate of Analysis	Dec 30, 2021	D154231
B2210228	Certificate of Analysis	Dec 30, 2021	D154231
B2210271	Certificate of Analysis	Dec 30, 2021	D154231
B2210278	Certificate of Analysis	Dec 30, 2021	D154231
F2326099	Certificate of Analysis	Dec 30, 2021	D154231
G2402138	Certificate of Analysis	Dec 30, 2021	D154231

Show more⌵

Chemical and Physical Properties

Solubility	Soluble in methanol. Insoluble in water
Sensitivity	light sensitive
Flash Point(°F)	>235.4 °F
Flash Point(°C)	>113 °C
Boil Point(°C)	286-288 °C
Melt Point(°C)	47-54°C
Molecular Weight	180.200 g/mol
XLogP3	1.800
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	3
Exact Mass	180.079 Da
Monoisotopic Mass	180.079 Da
Topological Polar Surface Area	35.500 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	179.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Yujie Qi, Xing Huang, Haoqi Zhai, Mengquan Shi, Yuxi Zhang, Yunlong Zhang, Yuxia Zhao. (2022) Synthesis and photoinitiation properties of lignin model compounds. PROGRESS IN ORGANIC COATINGS, 173 (107210).
2. Xia Zhang, Wenzhi Li, Yihang Jiang, Leyu Zhu, Liqun Wang. (2024) Valorization of waste lignin: Efficient and steady production of liquid fuels. INDUSTRIAL CROPS AND PRODUCTS, 220 (119400).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration

Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.