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193070

Sigma-Aldrich

2-Methylbutyric acid

98%

Synonym(s):

NSC 7304

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Estimated to ship onMarch 29, 2025


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25 G
¥3,900
100 G
¥7,100

About This Item

Linear Formula:
C2H5CH(CH3)CO2H
CAS Number:
Molecular Weight:
102.13
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
liquid
Assay:
98%

¥3,900

List Price¥6,620Save 41%

Estimated to ship onMarch 29, 2025


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vapor pressure

0.5 mmHg ( 20 °C)

Quality Level

Assay

98%

form

liquid

refractive index

n20/D 1.405 (lit.)

bp

176-177 °C (lit.)

density

0.936 g/mL at 25 °C (lit.)

functional group

carboxylic acid

SMILES string

CCC(C)C(O)=O

InChI

1S/C5H10O2/c1-3-4(2)5(6)7/h4H,3H2,1-2H3,(H,6,7)

InChI key

WLAMNBDJUVNPJU-UHFFFAOYSA-N

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General description

2-Methylbutyric acid is a short-chain fatty acid used as a chemical intermediate for plasticizers and lubricants.[1]

Enantioselective esterification of (+/-)-2-methylbutynic acid catalyzed by Chromobacterium viscosum lipase immobilized in microemulsion-based organogels has been investigated[2].

Application

2-Methylbutyric acid was used in the synthesis of 2-methylbutyric anhydride, an acylating agent[3].

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

170.6 °F - closed cup

Flash Point(C)

77 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

193070-VAR:
193070-BULK:
193070-100G:
193070-25G:


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Enantioselective esterification of 2-methylbutyric acid catalyzed via lipase immobilized in microemulsion-based organogels.
Uemasu I and Hinze WL.
Chirality, 6(8), 649-653 (1994)
Different acylating agents in the synthesis of aromatic ketones on sulfated zirconia.
Deutsch J, et al.
Catalysis Letters, 88(1-2), 9-15 (2003)
Production of C5 carboxylic acids in engineered Escherichia coli
Dhande YK, et al.
Process Biochemistry (Oxford, United Kingdom), 47, 1965-1971 (2012)
Annika Cichy et al.
Current biology : CB, 29(16), 2687-2697 (2019-08-06)
The mammalian main olfactory pathway detects myriad volatile chemicals using >1,000 odorant receptor (OR) genes, which are organized into two phylogenetically distinct classes (class I and class II). An important question is how these evolutionarily conserved classes contribute to odor
G Hayashida-Soiza et al.
Journal of applied microbiology, 105(5), 1672-1677 (2008-10-03)
To purify and characterize compounds with antimicrobial activity from Pseudoalteromonas haloplanktis inhibition (INH) strain. The P. haloplanktis isolated from a scallop hatchery was used to analyse antibacterial activities. Crude extracts were obtained with ethyl acetate of the cultured broth, after

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