CAS 103-49-1|Dibenzylamine

Introduction:Basic information about CAS 103-49-1|Dibenzylamine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameDibenzylamine
CAS Number103-49-1Molecular Weight197.28
Density1.0±0.1 g/cm3Boiling Point300.0±0.0 °C at 760 mmHg
Molecular FormulaC14H15NMelting Point−26 °C(lit.)
MSDSChineseUSAFlash Point143.3±0.0 °C
Symbol
GHS05, GHS07
Signal WordDanger

Names

NameDibenzylamine
SynonymMore Synonyms

Dibenzylamine BiologicalActivity

DescriptionDibenzylamine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related CatalogResearch Areas >>Others
In Vitro二苄胺是一种强大的神经生成剂的成分。

Chemical & Physical Properties

Density1.0±0.1 g/cm3
Boiling Point300.0±0.0 °C at 760 mmHg
Melting Point−26 °C(lit.)
Molecular FormulaC14H15N
Molecular Weight197.28
Flash Point143.3±0.0 °C
Exact Mass197.120453
PSA12.03000
LogP3.42
Vapour Pressure0.0±0.6 mmHg at 25°C
Index of Refraction1.581
InChIKeyBWLUMTFWVZZZND-UHFFFAOYSA-N
SMILESc1ccc(CNCc2ccccc2)cc1
StabilityStable. Incompatible with oxidizing agents, acid anhydrides, acids, acid chlorides, chloroformates.
Water Solubility0.05 g/L (20 ºC)

Safety Information

Symbol
GHS05, GHS07
Signal WordDanger
Hazard StatementsH302-H314
Precautionary StatementsP280-P305 + P351 + P338-P310
Personal Protective EquipmentFaceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard CodesC:Corrosive
Risk PhrasesR22;R34;R52/53
Safety PhrasesS26-S61-S45-S36/37/39
RIDADR2810
WGK Germany3
Packaging GroupIII
Hazard Class8
HS Code2921499090

Customs

HS Code2921499090
Summary2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles24

More Articles
Spectrophotometric determination of folic acid in pharmaceutical preparations by coupling reactions with iminodibenzyl or 3-aminophenol or sodium molybdate-pyrocatechol.

Anal. Biochem. 307(2) , 316-21, (2002)

Novel coupling reagents are used for the simple and sensitive spectrophotometric determination of folic acid either in pure form or in its pharmaceutical preparations. The methods are based on the pro...

Diastereoselective construction of syn-α-oxyamines via three-component α-oxyaldehyde-dibenzylamine-alkyne coupling reaction: application in the synthesis of (+)-β-conhydrine and its analogues.

Org. Biomol. Chem. 10(37) , 7536-44, (2012)

A Cu(I)-catalyzed α-oxyaldehyde-dibenzylamine-alkyne coupling reaction was delineated for the construction of α-oxyamines with excellent yields and diastereoselectivity. Crystal structure analysis and...

Kinetic study on the nitrosation of dibenzylamine in a model system.

Food Chem. Toxicol. 32(11) , 1015-9, (1994)

A kinetic study of the formation of N-nitrosodibenzylamine (NDBzA), from the nitrosation of dibenzylamine (DBzA) by sodium nitrite, was performed in a model system under conditions (temperature, pH) t...

Synonyms

bis-benzylamine
Dibenzylamine
Bibenzylamine
dibenzyl-amine
PhCH2NHCH2Ph
Benzenemethanamine, N-(phenylmethyl)-
DIBAM
Benzenemethanamine, N- (phenylmethyl)-
forLabetalol
(N-Benzylaminomethyl)benzene
MFCD00004770
EINECS 203-117-7
N-Benzylbenzylamine
di-benzylamine
Vulcaid 28
N,n-dibenzylamine
N-Benzyl-1-phenylmethanamine
DBZA
N-(Phenylmethyl)benzenemethanamine
Accelerator DBA
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