ISOBUTYL FORMATE (542-55-2)

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Suppliers

• Sigma-Aldrich - ISOBUTYL FORMATE
  40.00 - 749.00 USD
• Fisher Scientific - Search for ISOBUTYL FORMATE
• TCI - ISOBUTYL FORMATE
  20.00 - 117.00 USD

Most-cited Publications

• Physical Properties of Binary Mixtures of Ethyl Formate with Benzene, Isopropyl Benzene, Isobutyl Benzene, and Butylbenzene at (303.15, 308.15, and 313.15) K (Journal of Chemical & Engineering Data, 2010)
• Isobaric VaporLiquid Equilibrium for Binary Systems of Thioglycolic Acid with Water, Butyl Acetate, Butyl Formate, and Isobutyl Acetate at 101.3 kPa (Journal of Chemical & Engineering Data, 2017)
• Assessment, measurement and correlation of (vapour + liquid) equilibrium of (carbon dioxide + butyl, isobutyl, and amyl formate) systems (The Journal of Chemical Thermodynamics, 2013)
• Vapour-liquid equilibrium in the isobutyl formate-isobutyl alcohol and n-butyl formate-isobutyl alcohol systems at atmospheric pressure (Collection of Czechoslovak Chemical Communications, 1979)
• Reactions of OH and Cl with isopropyl formate, isobutyl formate, n-propyl isobutyrate and isopropyl isobutyrate (Chemical Physics Letters, 2014)
• XXX. The magneto-optical dispersion of organic liquids in the ultra-violet region of the spectrum.Part VII. The magneto-optical dispersion of isobutyl formate, methyl butyrate, and ethyl malonate (Philosophical Magazine Series 1, 1934)

Safety

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• H225: Highly Flammable liquid and vapor
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• H335: May cause respiratory irritation
  Warning Specific target organ toxicity, single exposure; Respiratory tract irritation - Category 3

Trends

Alternate Names

• SMILES
  CC(C)COC=O
• InChIKey
  AVMSWPWPYJVYKY-UHFFFAOYSA-N

External Links

• Pubchem - ISOBUTYL FORMATE
• Wikipedia - isobutyl formate
  Isobutyl formate (2-methylpropyl methanoate) is an organic ester with the chemical formula C5H10O2. It is formed by diluting isobutanol with formic acid; sulfuric acid can serve as a catalyst. It is used as a flavor and fragrance ingredient because of its odor which is sweet, ethereal, and slightly fruity.

Synthesis

formic acid  +  1-Chloro-2-methylpropane (Ester from carboxilic acid(SN2))

Isobutoxymethanol  +  dimethyl sulfide (Corey-Kim oxidation of secondary alcohols)

Synthesis of ISOBUTYL FORMATE ›

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4-METHYL-1-PENTENE (691-37-2, 25068-26-2)

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5-Methyl-1-hexene (68975-47-3, 3524-73-0)

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Hexanal (66-25-1)

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1-Methoxy-2-propanol (107-98-2)

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2,3-DIMETHYLBUTANE (75-83-2, 79-29-8, 107-83-5, 96-14-0)

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METHACROLEIN (4170-30-3, 78-85-3)

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1-BROMO-3-METHYLBUTANE (107-82-4)

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2-(Hexyloxy)ethanol (31726-34-8, 112-25-4)

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2-METHYL-3-BUTEN-2-OL (115-18-4)

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2-METHYL-3-BUTYN-2-OL (115-19-5)

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cis-3-Hexenal (6789-80-6)

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tert-Butyl methyl ether (1634-04-4)

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butyraldehyde (123-72-8)

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Diisopropyl ether (108-20-3)

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ISOBUTANE (75-28-5)

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DIISOPROPYLAMINE (110-97-4, 108-18-9)

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ISOPROPYL ACETATE (108-21-4)

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ETHYL FORMATE (109-94-4)

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3-METHYL-2-BUTANONE (563-80-4)

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5-METHYL-2-HEXANONE (110-12-3)

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(Z)-Hex-3-en-1-ol (928-96-1, 928-97-2)

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ISOBUTYL FORMATE

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