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Benzhydrylimine

Benzhydrylimine

CAS: 1013-88-3

Molecular Formula: C13 H11 N

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Benzhydrylimine - Names and Identifiers

Name Benzhydrylimine
Synonyms Benzhydrylimine
BENZOPHENONIMINE
Benzophone imine
BENZOPHENONE IMINE
DIPHENYLMETHANIMINE
BENZHYDRYLIDENEAMINE
1,1-diphenylmethanimine
DiphenylMethaniMineiMine
Benzenemethanimine,-phenyl-
6-benzoylcyclohexa-2,4-dien-1-iMine
1-naphtholphthalein.BenzophenoneiMine
1,1-Diphenylmethylimine, Benzophenone imine, 1,1-Diphenylmethanimine
CAS 1013-88-3
InChI InChI=1/C13H11N/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,14H
InChIKey SXZIXHOMFPUIRK-UHFFFAOYSA-N

Benzhydrylimine - Physico-chemical Properties

Molecular FormulaC13 H11 N
Molar Mass181.23
Density1.08g/mLat 25°C(lit.)
Melting Point-30 °C
Boling Point151-153°C10mm Hg(lit.)
Flash Point145 °C
Water Solubility0.3 g/L (25 ºC)
Solubility DMSO (Slightly), Ethyl Acetate (Slightly)
Vapor Presure0.082Pa at 20℃
AppearanceLiquid
ColorClear colorless to light yellow-brownish
BRN1100371
pKapK1:6.82 (25°C)
Storage ConditionInert atmosphere,Room Temperature
Refractive Indexn20/D 1.618(lit.)
Physical and Chemical PropertiesMelting Point -30°C
boiling point 151-153 ° C 10mm Hg(lit.)

density 1.08g/mL at 25°C(lit.)

refractive index n20/D 1.618(lit.)

flash point 145°C
solubility in water 0.3g/L (25°C)

Benzhydrylimine - Risk and Safety

Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 
R38 - Irritating to the skin
R22 - Harmful if swallowed
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. 
S37 - Wear suitable gloves.
UN IDsUN3082
WGK Germany3
HS Code29252900

Benzhydrylimine - Reference Information

NIST chemical information information provided by: webbook.nist.gov (external link)
Application benzophenone imine is a commonly used reagent that can be used as a protecting group for primary amines. In particular, it is widely used in amino acid chemistry and can also be reacted with aryl halides to prepare aromatic amines.
Use for organic synthesis.
production method benzophenone oxime is heated and decomposed to generate benzophenone and benzophenone imine, and dry hydrogen chloride gas is introduced into the reaction mixture, the benzophenone imine is precipitated into a salt, the imine salt is filtered out, and then neutralized with a base to obtain free benzophenone imine.
Last Update:2024-04-09 21:04:16
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View History
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