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About This Item
grade
synthesis grade
Quality Segment
vapor pressure
20 hPa ( 20 °C)
form
liquid
potency
1136 mg/kg LD50, oral (Rat)
reaction suitability
reagent type: oxidant
pH
12-13 (20 °C in H2O)
bp
≥100 °C/1013 hPa
mp
<-3 °C
density
1.20-1.25 g/cm3 at 20 °C
storage temp.
2-30°C
Application
- Aldehydes to corresponding carboxylic acids under mild reaction conditions in the presence of scavengers such as sulfamic acid or resorcinol.
- Primary alcohols to carboxylic acids in the presence of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) and NaOCl.
- Aliphatic and aromatic thiols to the corresponding disulfides.
- Aryl boronic acids to phenols via ipso-hydroxylation.
- Cyclic benzylic ethers and N-protected cyclic benzylic amines to benzolactones and benzolactams.
- Alkenes to epoxides using aldehydes as promoters.
- Alkenes and cycloalkenes to 1, 2 diols via osmium-catalyzed Sharpless asymmetric dihydroxylation.
It can also be used in combination with Br2 to synthesize 2-carboxyazetidin-2-ones from furanylazetidinones.
Analysis Note
Density (d 20 °C/ 4 °C): 1.200 - 1.220
signalword
Danger
target_organs
spleen
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1 - STOT RE 2
supp_hazards
Storage Class
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
Regulatory Listings
Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.
Deleterious substance
pdsc
Substances Subject to be Indicated Names
ishl_indicated
Substances Subject to be Notified Names
ishl_notified
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