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179981

Sigma-Aldrich

Luperox® A98, Benzoyl peroxide

reagent grade, ≥98%

Sinonimo/i:

Benzoyl peroxide, Dibenzoyl peroxide

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About This Item

Formula condensata:
(C6H5CO)2O2
Numero CAS:
Peso molecolare:
242.23
Beilstein:
984320
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.21
Stato:
solid
Saggio:
≥98%
Prezzi e disponibilità al momento non sono disponibili

Grado

reagent grade

Livello qualitativo

Saggio

≥98%

Stato

solid

Temp. autoaccensione

176 °F

Impiego in reazioni chimiche

reagent type: oxidant

Punto di fusione

105 °C (lit.)

Gruppo funzionale

peroxide
phenyl

Stringa SMILE

O=C(OOC(=O)c1ccccc1)c2ccccc2

InChI

1S/C14H10O4/c15-13(11-7-3-1-4-8-11)17-18-14(16)12-9-5-2-6-10-12/h1-10H
OMPJBNCRMGITSC-UHFFFAOYSA-N

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Descrizione generale

Benzoyl peroxide participates in the covalent insitu functionalization of carbon nanotubes. On heating, it undergoes decomposition to afford phenyl free radicals and CO2 gas.[1]
Luperox® A98, Benzoyl peroxide, an anhydrous benzoyl peroxide powder, is a mainly used as a thermal free radical initiator in polymerization reactions.

Applicazioni

Benzoyl peroxide has been used as an initiator in the preparation of the following:
  • Thermal cross-linking of multiwalled carbon nanotubes (MWCNTs) via radical-initiated reaction[1]
  • 3-D crosslinked carbon scaffolds[1]
  • poly(lactic-co-glycolic) acid (PLGA), MWCNT and singlewalled carbon nanotubes (SWCNT) scaffolds[2]
Widely used initiator, curing agent, and cross-linking agent in polymerization processes.

Note legali

Product of Arkema Inc.
Luperox is a registered trademark of Arkema Inc.

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Org. Perox. B - Skin Sens. 1A

Codice della classe di stoccaggio

4.1A - Other explosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Gaurav Lalwani et al.
Carbon, 53, 90-100 (2013-02-26)
We report a simple method to fabricate macroscopic, 3-D, free standing, all-carbon scaffolds (porous structures) using multiwalled carbon nanotubes (MWCNTs) as the starting materials. The scaffolds prepared by radical initiated thermal crosslinking, and annealing of MWCNTs possess macroscale interconnected pores
Suzanne M Jervis et al.
Journal of food science, 78(2), R129-R137 (2013-01-22)
Whey is a value-added product that is utilized in many food and beverage applications for its nutritional and functional properties. Whey and whey products are generally utilized in dried ingredient applications. One of the primary sources of whey is from
E J Kang et al.
Journal of food science, 77(7), C818-C823 (2012-07-05)
Residual annatto colorant (norbixin) in fluid Cheddar cheese whey can be bleached. The 2 approved chemical bleaching agents for whey, hydrogen peroxide (HP) and benzoyl peroxide (BP), negatively impact the flavor of dried whey protein. The objective of this study
Adam J Friedman et al.
The Journal of investigative dermatology, 133(5), 1231-1239 (2012-11-30)
Advances in nanotechnology have demonstrated potential application of nanoparticles (NPs) for effective and targeted drug delivery. Here we investigated the antimicrobial and immunological properties and the feasibility of using NPs to deliver antimicrobial agents to treat a cutaneous pathogen. NPs
Emil A Tanghetti et al.
Dermatologic clinics, 27(1), 17-24 (2008-11-06)
Benzoyl peroxide (BPO) is the most widely used topical acne treatment, with significant antibacterial, antikeratolytic, and comedolytic activity. It has been shown to be extremely effective as monotherapy and in combination with antibiotics or retinoids for managing comedonal and inflammatory

Questions

  1. What analytical procedure is used to evaluate the purity of Luperox® A98, Benzoyl peroxide (#179981)?

    1 answer
    1. This item is a product of Arkema. The manufacturer considers the assay method proprietary. However, the protocol is based on the following reference:
      Atochem Research Notebook 7032: 3, 5
      A. G. McFarland, Research Progress Report: "Iodometric Determination of Benzoyl Peroxide", 2/18/91

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