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Performic Acid, also known as peroxyformic acid, is a colorless liquid with unstable solutions. It is a powerful oxidizing agent that is commonly used in various chemical reactions, particularly in the fields of organic synthesis and epoxidation.

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  • 107-32-4 Structure
  • Basic information

    1. Product Name: Performic Acid
    2. Synonyms: peroxyformic acid;Hydroperoxyformaldehyde;peroxymethanoic acid;Methaneperoxoic acid(9CI)
    3. CAS NO:107-32-4
    4. Molecular Formula: CH2O3
    5. Molecular Weight: 62.03
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107-32-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 127.5°Cat760mmHg
    3. Flash Point: 67.5°C
    4. Appearance: /
    5. Density: 1.341g/cm3
    6. Vapor Pressure: 5.09mmHg at 25°C
    7. Refractive Index: 1.357
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. Water Solubility: miscible with H2O, alcohol, ether; soluble benzene, chloroform [HAW93]
    11. CAS DataBase Reference: Performic Acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: Performic Acid(107-32-4)
    13. EPA Substance Registry System: Performic Acid(107-32-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 107-32-4(Hazardous Substances Data)

107-32-4 Usage

Uses

Used in Chemical Synthesis:
Performic Acid is used as an epoxidizing agent and in organic synthesis for oxidation and hydroxylation reactions. It is particularly effective in the conversion of alkenes to epoxides and the introduction of hydroxyl groups into organic molecules.
Used in Oxidation Reactions:
Performic Acid is used as an oxidizing agent in various chemical processes. Its strong oxidizing properties make it suitable for a wide range of oxidation reactions, including the conversion of alcohols to aldehydes, ketones, or carboxylic acids.
Used in Epoxidation Reactions:
Performic Acid is used as an epoxidizing agent in the conversion of alkenes to epoxides. This reaction is particularly useful in the synthesis of various chemicals and pharmaceuticals, as epoxides serve as important intermediates in the production of numerous compounds.
Used in Hydroxylation Reactions:
Performic Acid is used for hydroxylation reactions, where it introduces hydroxyl groups into organic molecules. This is particularly useful in the synthesis of various chemicals, as the introduction of hydroxyl groups can significantly alter the properties and reactivity of the molecule.

Health Hazard

Peroxyformic acid is nontoxic. It is a skinand eye irritant. Its irritant action is lesssevere than that of peroxyacetic acid. Thereare no reports on its tumorigenic properties.

Fire Hazard

Peroxyformic acid is the only oxygen-balanced organic peroxide. Its active oxygen content (25.8%) is greater than that of other peroxy compounds. It is therefore expected to undergo extremely violent decomposition. However, in practice, this compound forms only in situ and the commercial formulations contain its aqueous or dilute solutions in organic solvents.The solutions of peroxyformic acid are shock and heat sensitive and highly reactive and decompose violently when exposed to heat. Dilution with water increases the sensitivity to shock and heat. It is a strong oxidizer and may react violently with readilyoxidizable substances. It may ignite and explodes when mixed with accelerators or flammable substances. Peroxyformic acid at 60% strength can react violently with formaldehyde, benzaldehyde, aniline, powdered aluminum, and lead dioxide (NFPA 1986). Water from a sprinkler system may be used from an explosion-resistant location to fight fire and keep the containers cool. .

Safety Profile

A powerful irritant and an oxidizer. A dangerous fire hazard when exposed to heat, flame, or reducing materials. Unstable and shock-sensitive. 80% solution is explosive. Extremely dangerous when moved. Violent reaction with carbon, red phosphorus, silicon

Waste Disposal

The spilled solution of peroxyformic acidshould be absorbed by vermiculite or othernoncombustible absorbent and disposed ofimmediately. Do not use paper, wood, orspark-generating metals for sweeping andhandling. It is destroyed by burning on theground in a remote place using a long torch.Concentrated aqueous solutions in a smallquantity may be diluted with copious quantities of water and flushed down the drain.

Check Digit Verification of cas no

The CAS Registry Mumber 107-32-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 107-32:
(5*1)+(4*0)+(3*7)+(2*3)+(1*2)=34
34 % 10 = 4
So 107-32-4 is a valid CAS Registry Number.
InChI:InChI=1/CH2O3/c2-1-4-3/h1,3H

107-32-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name peroxyformic acid

1.2 Other means of identification

Product number -
Other names Performic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107-32-4 SDS

107-32-4Related news

CATALYSIS, KINETICS AND REACTORSKinetics of Formic Acid-autocatalyzed Preparation of Performic Acid (cas 107-32-4) in Aqueous Phase08/22/2019

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Chemical disinfection of combined sewer overflow waters using Performic Acid (cas 107-32-4) or peracetic acids08/21/2019

We investigated the possibility of applying performic acid (PFA) and peracetic acid (PAA) for disinfection of combined sewer overflow (CSO) in existing CSO management infrastructures. The disinfection power of PFA and PAA towards Escherichia coli (E. coli) and Enterococcus was studied in batch-s...detailed

Process intensification using a spiral capillary microreactor for continuous flow synthesis of Performic Acid (cas 107-32-4) and it’s kinetic study08/20/2019

The continuous production of performic acid is getting significant importance due to it’s versatile oxidizing properties in various applications such as in the food, oil and chemical industries. In this work, an attempt has been made for synthesis of performic acid in a continuous flow microrea...detailed

107-32-4Relevant articles and documents

Kinetics of formation of peroxyformic acid

Mosovsky, Vladimir,Cvengrosova, Zuzana,Kaszonyi, Alexander,Kralik, Milan,Hronec, Milan

, p. 1457 - 1463 (1996)

Oxidation kinetics of formic acid with aqueous hydrogen peroxide (30-70%) has been studied at 45°C with 0-0.1 M H2SO4 as a catalyst. A kinetic model has been suggested which satisfactorily describes the oxidation process of formic acid to peroxyformic acid.

33. Synthesis of Concentrated 18O-Labelled Hydrogen Peroxide and of 2H-, 13C- and 18O-Labelled Peroxyformic Acid

Grassi, Guido,Oldani, Markus,Bauder, Alfred

, p. 400 - 404 (1983)

A method is described for the preparation of concentrated solutions (50-70percent) of 18O-labelled H2O2 in water.All singly 2H-, 13C- and 18O-labelled species of peroxyformic acid have been synthesized by the reaction of appropriately labelled formic acid and H2O2.

Quantitation of glutathione and its oxidation products in erythrocytes by multiple-label stable-isotope dilution

Reinbold, Julia,Koehler, Peter,Rychlik, Michael

, p. 41 - 48 (2014)

A multiple-label stable isotope dilution assay for quantifying glutathione (GSH), glutathione disulfide (GSSG), and glutathione sulfonic acid in erythrocytes was developed. As the internal standards, [13C 3,15N]glutathione

Unexpected reaction of melatonin derivatives with performic acid

Mol?da, Zuzanna,Zawadzka, Anna,Zytek, Ma?gorzata,Madej, Daria,Pluciński, Franciszek,Maurin, Jan K.,Czarnocki, Zbigniew

, p. 807 - 813 (2013)

A series of carbamate melatonin derivatives was treated with performic acid, providing tricyclic products with a 3-hydroxytetrahydropyrrolo[2,3-b] indole skeleton. An unusual migration of carbamate groups was observed in some cases, and the reaction appea

Vibrational spectra and normal coordinate analysis of isotopically labelled peroxyformic acid.

Tyblewski, M.,Dommen, J.,Ha, T.-K.,Bauder, A.

, p. 397 - 408 (1991)

Infrared spectra of peroxyformic acid (HCOOOH) and the six isotopic modifications H13COOOH, HC18OOOH, DCOOOH, HCOOOD, H13COOOD, DCOOOD have been recorded in an argon matrix in the spectral range 200-4000 cm-1.Assignments of the observed absorpt

The benzoin condensation: Charge tagging of the catalyst allows for tracking by mass spectrometry Dedicated to Professor Veronica M. Bierbaum.

Zeng, Hao,Wang, Kai,Tian, Yuan,Niu, Yijie,Greene, Landon,Hu, Zhichao,Lee, Jeehiun K.

, p. 92 - 97 (2014)

A novel thiazolium with a sulfonate charge tag was synthesized to test the feasibility of tracking the progress of a thiazolylidene-catalyzed benzoin condensation reaction using electrospray ionization-mass spectrometry (ESI-MS). Intermediates in the benz

Microwave Spectrum, Dipole Moment, and Substitution Structure of Peroxyformic Acid

Oldani, M.,Ha, T.-K.,Bauder, A.

, p. 360 - 365 (1983)

The microwave spectra of peroxyformic acid (HCOOOH) and seven isotopic species have been investigated from 12 to 40 GHz.Rotational constants and all quartic centrifugal distortion constants have been adjusted from measured transition frequencies for the p

Photooxidation of Formaldehyde in Solid Oxygen and Argon/Oxygen Matrices at 12 K

Diem, Michael,Lee, Edward K. C.

, p. 4507 - 4512 (1982)

Matrix-isolated formaldehyde in solid O2, Ar/O2, and Ar matrices at 12 K has been photolyzed by ultraviolet light in the 220 - 400 nm range.The photoproducts were identified by infrared spectroscopy.Stable oxidation products were CO, CO2, H2O, H2O2, O3, and HCOOH, whereas relatively unstable products were HO2, its hydrogen-bonded dimer (HO2)2, formylperoxy radical HC(O)OO, and performic acid.The observed photoproduct distribution is rationalized by the stoichiometry of chemical reactions involving one C atom, two H atoms, and odd numbers of O atoms in the cage.Photolysis of the Ar/O2/H2CO sample (10 percent O2 in solid Ar) gave poor yields of radical species.Under the experimental conditions employed, the photochemical oxidation process is not driven to completion, and therefore it is possible to trap reactive intermediates for spectroscopic and kinetic studies.Photodissociation threshold of H2CO and (H2CO)2 in solid Ar have been measured with tunable, pulsed UV laser photolysis to show that (H2CO)2 has a lower treshold than H2CO.

Enzymatic synthesis and characterization of L-methionine and 2-hydroxy-4-(methylthio)butanoic acid (HMB) co-oligomers

Rajesh, Mathur,Kapila, Shubhen,Nam, Paul,Forciniti, Daniel,Lorbert, Stephen,Schasteen, Charles

, p. 2461 - 2467 (2003)

Oligomers of L-methionine (Met) and its hydroxy analogue, 2-hydroxy-4-(methylthio)butanoic acid (D,L-HMB) were synthesized with the proteolytic enzyme papain. The Met homooligomers and HMB-Met co-oligomers obtained through the enzymatic reactions were sub

Quantitative analysis of oxidized vitamin B1 metabolites generated by hypochlorous acid

Sasatsuki, Hitoshi,Nakazaki, Atsuo,Uchida, Koji,Shibata, Takahiro

, p. 197 - 206 (2020)

Thiamine, a water-soluble essential vitamin known as vitamin B1, acts as an important cofactor in various cellular processes, such as metabolism and energy production. Thiamine is also thought to have antioxidant effects as a singlet oxygen scavenger and

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