537349

Ethyl acetoacetate

ReagentPlus®, 99%

Manufacturer: Sigma Aldrich

CAS Number: 141-97-9

Synonym(S): EAA, Ethyl 3-oxobutanoate, Acetoacetic ester

Select a Size

Pack Size SKU Availability Price
1 KG 537349-1-KG In Stock ₹ 3,160.00
3 KG 537349-3-KG In Stock ₹ 7,794.00

537349 - 1 KG

₹ 3,160.00

In Stock

Quantity

1

Base Price: ₹ 3,160.00

GST (18%): ₹ 568.80

Total Price: ₹ 3,728.80

vapor density

4.48 (vs air)

Quality Level

200

vapor pressure

1 mmHg ( 28.5 °C)

product line

ReagentPlus®

Assay

99%

autoignition temp.

580 °F

expl. lim.

9.5 %

bp

181 °C (lit.)

mp

−43 °C (lit.)

solubility

water: soluble 130 g/L at 20 °C

Other Options

Image Product Name Manufacturer Price Range
Ethyl acetoacetate, ≥99% (GC), MilliporeSigma™ Supelco™
-- ₹ 8,099.00
Sigma Aldrich Fine Chemicals Biosciences Ethyl acetoacetate natural, >=97%, FG | 141-97-9 | MFCD00009199 | 100G
-- ₹ 7,449.30
Sigma Aldrich Fine Chemicals Biosciences Ethyl acetoacetate puriss. p.a., >=99.0% (GC) | 141-97-9 | MFCD00009199 | 100ML
-- ₹ 5,963.00
Ethyl acetoacetate
-- ₹ 5,358.38 - ₹ 92,402.20
Ethyl acetoacetate
-- ₹ 5,152.70 - ₹ 41,373.15
Ethyl acetoacetate
-- ₹ 3,496.48 - ₹ 11,106.45
Ethyl acetoacetate
-- ₹ 12,145.65 - ₹ 2,81,828.88
Butanoic acid, 3-oxo-, ethyl ester
-- ₹ 267.00 - ₹ 356.00
Ethyl acetoacetate
-- ₹ 2,047.00 - ₹ 4,005.00
141-97-9 | Ethyl acetoacetate
-- ₹ 445.00 - ₹ 1,691.00

Related Products

Img

Sigma Aldrich

538051

≥99.6%...

Img

Sigma Aldrich

538728

ReagentPlus®, ≥99.8%...

Img

Sigma Aldrich

471305

99.5%...

Img

Sigma Aldrich

52828

ReagentPlus®, ≥99.5% (GC)...

Img

Sigma Aldrich

471577

≥99%...

Img

Sigma Aldrich

493732

ReagentPlus®, 99%...

Img

Sigma Aldrich

525200

99%...

Img

Sigma Aldrich

538205

dry, 98%...

Description

  • Application: Ethyl acetoacetate is a versatile reagent that can be used as a nucleophile in alkylation, conjugate addition and condensation reactions.[1] Some of its applications are:Alkylation at the α-carbon of ethyl acetoacetate followed by hydrolysis and decarboxylation can afford a variety of methyl ketones.[2] It also undergoes acylation at the α-carbon in the presence of MgCl2 and pyridine to give synthetically important intermediates.[3]It can be used in Knoevenagel condensation with aliphatic, aromatic, and heteroaromatic aldehydes to produce α-alkylideneacetoacetates.[1][4]
  • Legal Information: ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

SAFETY INFORMATION

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves