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513474

Sigma-Aldrich

Luperox® A75FP, Benzoyl peroxide

contains 25 wt. % water as stabilizer, 75%

Sinónimos:

Benzoyl peroxide moistened with water, BPO, Benzoyl peroxide, Diacyl peroxide, Dibenzoyl peroxide

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About This Item

Fórmula lineal:
(C6H5CO)2O2
Peso molecular:
242.23
Beilstein/REAXYS Number:
984320
MDL number:
MFCD00003071
UNSPSC Code:
12162002
PubChem Substance ID:
24873694
NACRES:
NA.23

product name

Luperox® A75FP, Benzoyl peroxide, 75% remainder water, contains 25 wt. % water as stabilizer, 75%

assay

75%

form

powder

contains

25 wt. % water as stabilizer

reaction suitability

reagent type: oxidant

mp

103 °C (lit.)

storage temp.

2-8°C

SMILES string

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

InChI key

OMPJBNCRMGITSC-UHFFFAOYSA-N

Other Notes

Self Accelerating Decomposition Temperature (SADT): 71 °C

Legal Information

Luperox is a registered trademark of Arkema Inc.

signalword

Danger

Hazard Classifications

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

Storage Class

4.1A - Other explosive hazardous materials

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
MKCN7323
MKCN7321
MKCM2903
MKCJ7446
MKCM4625

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To increase colonoscopy capability to discriminate benign from malignant polyps, we suggest combining two imaging approaches based on targeted polymeric platforms. Water-soluble cationized polyacrylamide (CPAA) was tagged with the near infrared (NIR) dye IR-783-S-Ph-COOH to form Flu-CPAA. The recognition peptide
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Late-onset fragility fractures are a common complication following radiotherapy for metastatic disease and soft tissue sarcomas. Using a murine hindlimb focal irradiation model (RTx), we quantified time-dependent changes in osteoclasts and mineral apposition rate (MAR). Mice received either a single
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An alternative strategy for surface tethering of DNA probes, where highly reactive glassy carbon (GC) substrates are prepared via electrochemical hydrogenation and electrochemical/chemical chlorination is reported. Thiolated DNA probes and alkanethiols were stably immobilised on the halogenated carbon, with electrochemical
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