Basic Description

Synonyms	1-Methoxyacetone \| Methoxymethyl methyl ketone \| Methoxy-2-propanone \| 1-Methoxy-2-propanone \| BRN 1560175 \| MFCD00008768 \| ZHQ6G2H7L3 \| 1-Methoxy-propan-2-one \| EINECS 227-549-0 \| methoxyaceton
Specifications & Purity	≥96%(GC)
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organooxygen compounds
    - Subclass Carbonyl compounds

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organooxygen compounds
Subclass	Carbonyl compounds
Intermediate Tree Nodes	Not available
Direct Parent	Ketones
Alternative Parents	Dialkyl ethers Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Ketone - Ether - Dialkyl ether - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol.
External Descriptors	Not available
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

Names and Identifiers

Pubchem Sid	504753068
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504753068
IUPAC Name	1-methoxypropan-2-one
INCHI	InChI=1S/C4H8O2/c1-4(5)3-6-2/h3H2,1-2H3
InChIKey	CUZLJOLBIRPEFB-UHFFFAOYSA-N
Smiles	CC(=O)COC
Isomeric SMILES	CC(=O)COC
WGK Germany	3
RTECS	UC2988600
Molecular Weight	88.11
Beilstein	1560180
Reaxy-Rn	1560175
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1560175&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.

11 results found

Lot Number	Certificate Type	Date	Item
F2401002	Certificate of Analysis	May 21, 2024	M158844
F2403092	Certificate of Analysis	May 21, 2024	M158844
F2403093	Certificate of Analysis	May 21, 2024	M158844
F2403094	Certificate of Analysis	May 21, 2024	M158844
F23161501	Certificate of Analysis	Jun 26, 2023	M158844
F23161498	Certificate of Analysis	Jun 26, 2023	M158844
F23161504	Certificate of Analysis	Jun 26, 2023	M158844
L2206880	Certificate of Analysis	Oct 17, 2022	M158844
L2206528	Certificate of Analysis	Oct 17, 2022	M158844
L2206735	Certificate of Analysis	Oct 17, 2022	M158844
G1803099	Certificate of Analysis	May 07, 2022	M158844

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Chemical and Physical Properties

Sensitivity	Heat sensitive
Refractive Index	1.4
Flash Point(°F)	77.0 °F
Flash Point(°C)	25 °C
Boil Point(°C)	115 °C
Molecular Weight	88.110 g/mol
XLogP3	-0.200
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	88.0524 Da
Monoisotopic Mass	88.0524 Da
Topological Polar Surface Area	26.300 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	49.500
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. Hao Yan, Mingyue Zhao, Yueqiang Cao, Xin Zhou, Yibin Liu, Xiaobo Chen, Xiang Feng, Xuezhi Duan, Francisco Zaera, Xinggui Zhou, Chaohe Yang. (2024) Crystal-facet-dependent, electron sink effect for the enhanced selective oxidation of polyols at the secondary hydroxyl position. JOURNAL OF CATALYSIS, 431 (115401).
2. Hongjin Qu, Tianliang Lu, Xiaomei Yang, Lipeng Zhou. (2024) Promoting tin into the framework of β zeolite via stabilizing Sn species and its catalytic performance for the conversion of ethyl levulinate to γ-valerolactone. RENEWABLE ENERGY, 229 (120746).

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SKU	Size	Availability	Price
M158844-1ml	1ml	2	$26.90
M158844-5ml	5ml	3	$79.90
M158844-25ml	25ml	1	$269.90

Methoxyacetone - >96.0%(GC), high purity , CAS No.5878-19-3