B5907
Benzoyl peroxide blend with dicyclohexyl phthalate
suitable for use as a catalyst for electron microscopy. Modified to render it safe in transit.
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About This Item
Empirical Formula (Hill Notation):
C14H10O4
Molecular Weight:
242.23
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
MDL number:
Form:
powder
Quality Level
form
powder
contains
50% dicyclohexyl phthalate as stabilizer
reaction suitability
reagent type: oxidant
packaging
vial of 9.9 g
mp
54 °C
application(s)
diagnostic assay manufacturing
hematology
histology
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
Formulated specifically for use with Histocryl and LR white acrylic resins.
signalword
Danger
Storage Class
5.2 - Organic peroxides and self-reacting hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - ED HH 1 - Eye Irrit. 2 - Org. Perox. D - Repr. 1B - Skin Sens. 1
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Laszlo Prokai et al.
Science translational medicine, 7(297), 297ra113-297ra113 (2015-07-24)
Many neurological and psychiatric maladies originate from the deprivation of the human brain from estrogens. However, current hormone therapies cannot be used safely to treat these conditions commonly associated with menopause because of detrimental side effects in the periphery. The
Megan E Oest et al.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 33(3), 334-342 (2014-11-20)
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
Ahmed M Debela et al.
Biosensors & bioelectronics, 71, 25-29 (2015-04-17)
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