Advanced Search



Ethyl acetoacetate

ALDRICH/W241504 - ≥99%, FCC, FG

Synonym: Acetoacetic ester

CAS Number: 141-97-9
Empirical Formula (Hill Notation): C6H10O3
Molecular Weight: 130.14
EC Number: 205-516-1
MDL Number: MFCD00009199
Linear Formula: CH3COCH2COOC2H5
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-W241504-1KG-K 1 kg
$71.70
1/EA
Add To Favorites
45-W241504-5KG-K 5 kg
$182.00
1/EA
Add To Favorites
45-W241504-25KG-K 25 kg
$450.00
1/EA
Add To Favorites
45-W241504-SAMPLE-K
$54.60
1/EA
Add To Favorites

 

agency meets purity specifications of JECFA
application(s) flavors and fragrances
assay ≥99%
autoignition temp. 580 °F
biological source synthetic
bp 181 °C (lit.)
density 1.029 g/mL at 20 °C (lit.)
documentation see Safety & Documentation for available documents
expl. lim. 9.5 %
food allergen no known allergens
grade FG
  Kosher
InChI 1S/C6H10O3/c1-3-9-6(8)4-5(2)7/h3-4H2,1-2H3
InChI key XYIBRDXRRQCHLP-UHFFFAOYSA-N
mp −43 °C (lit.)
organoleptic apple; fatty; green; fruity
Quality Level 400 
refractive index n20/D 1.418-1.421
reg. compliance EU Regulation 1334/2008 & 178/2002
  FCC
  FDA 21 CFR 117
  FDA 21 CFR 172.515
SMILES string CCOC(=O)CC(C)=O
solubility water: soluble 130 g/L at 20 °C
vapor density 4.48 (vs air)
vapor pressure 1 mmHg ( 28.5 °C)
Application:

  • Fabrication of a novel magnetic nanostructure based on cellulose-gellan gum hydrogel, embedded with MgAl LDH as an efficient catalyst for the synthesis of polyhydroquinoline derivatives.: This study explores the use of ethyl acetoacetate in the synthesis of polyhydroquinoline derivatives, showcasing its application in developing efficient catalytic systems for organic reactions (Hjazi A, 2024 ).

  • Evaluation of diethyl 4-(5-bromo-1H-indol-3-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate: synthesis, anti-corrosion potential, and biomedical applications.: This research investigates the biomedical applications and anti-corrosion properties of compounds synthesized using ethyl acetoacetate, emphasizing its versatility in chemical synthesis and material science (Ahamed FMM et al., 2024 ).

  • Fe(3)O(4) nanoparticles impregnated eggshell as an efficient biocatalyst for eco-friendly synthesis of 2-amino thiophene derivatives.: The study highlights the use of ethyl acetoacetate in green chemistry, particularly in the eco-friendly synthesis of thiophene derivatives using biocatalysts (Zargari M et al., 2024 ).

  • Pyrano[2,3-c]pyrazole fused spirooxindole-linked 1,2,3-triazoles as antioxidant agents: Exploring their utility in the development of antidiabetic drugs via inhibition of α-amylase and DPP4 activity.: This paper discusses the synthesis of novel compounds with antidiabetic properties using ethyl acetoacetate, demonstrating its potential in drug development (Chahal S et al., 2024 ).

  • Access to Functionalized Cyclohex-2-enones from a Multicomponent Cascade Reaction of Readily Available Alkynes, Ketones, and Ethyl Acetoacetate.: The research details a multicomponent cascade reaction involving ethyl acetoacetate, highlighting its utility in the efficient synthesis of functionalized cyclohexenones (Jiang D et al., 2024 ).

Packaging: 1 kg in poly bottle
Packaging: 5, 25 kg in poly drum
WGK Germany WGK 1
Flash Point(F) 164.3 °F - closed cup
Flash Point(C) 73.5 °C - closed cup
Purity ≥99%
bp 181 °C (lit.)
mp −43 °C (lit.)
Density 1.029 g/mL at 20 °C (lit.)
Refractive Index n20/D 1.418-1.421
FEMA Number 2415
UNSPSC 12164502

The following items have been added to your cart:

Choose a favorite list for this item:

Catalog Number Description Price
$

Returns/Order support

Please fill out the form below if you want to request order support from Krackeler Scientific.


Quick Order

* Required


New Year Price Updates

We are currently working diligently to update our website pricing information for the New Year. If you place an order, you will be acknowledged with any corrected pricing. If you'd like the most current information sooner, please don't hesitate to drop us an email or give us a call and we'd be happy to assist. Thank you for your patience while we are updating.

800-334-7725
office@krackeler.com


Play Video

To Request a Quote

  1. Search or Browse for items and add to them to your Shopping Cart.
  2. Click the "Request Quote" button at the bottom of the Shopping Cart page.
  3. Fill out required fields.
  4. Optionally you can convert to standard checkout mode by choosing a payment type.
  5. Click "Request Quote" at the bottom of the page.

You will be contacted with a quote.

To Order From a Quote

  1. Register and login to the website.
  2. Receive a quote from your sales representative or customer service.
  3. Have your copy of the quote in hand.
  4. Visit our quote module to search for your quote.
Back to Top