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CAS NUMBER: 103-49-1
EC NUMBER: 203-117-7
MOLECULAR FORMULA: C14H15N
MOLECULAR WEIGHT: 197.27
DBZA (Di benzylamine) is an aromatic amine.
DBZA (Di benzylamine) is a primary aromatic amine consisting of a benzyl group and an amino group.
DBZA (Di benzylamine) is the simplest aromatic amine with the amino group in a side chain.
DBZA (Di benzylamine) is a strong base.
DBZA (Di benzylamine) is widely used in organic syntheses.
DBZA (Di benzylamine) is a precursor for the formation of diazonium salts.
DBZA (Di benzylamine) is an intermediate in the synthesis of a number of dyes and pigments , pharmaceuticals, agrochemicals, amino acids and other compounds.
DBZA (Di benzylamine) is also a corrosion inhibitor.
DBZA (Di benzylamine) is an organic chemical compound with the condensed structural formula C6H5CH2NH2 (sometimes abbreviated as PhCH2NH2 or BnNH2).
DBZA (Di benzylamine) consists of a benzyl group, C6H5CH2, attached to an amine functional group, NH2.
DBZA (Di benzylamine) is a common precursor in organic chemistry and used in the industrial production of many pharmaceuticals.
DBZA (Di benzylamine) can be produced by several methods, the main industrial route being the reaction of benzyl chloride and ammonia.
DBZA (Di benzylamine) is also produced by the reduction of benzonitrile and reductive amination of benzaldehyde.
DBZA (Di benzylamine) occurs biologically from the action of the N-substituted formamide deformylase enzyme.
DBZA (Di benzylamine) catalyses the conversion of N-benzylformamide into benzylamine with formate as a by-product.
DBZA (Di benzylamine) is degraded biologically by the action of the monoamine oxidase B enzyme, resulting in benzaldehyde.
DBZA (Di benzylamine) reacts with acetyl chloride to form N-benzylacetamide.
DBZA (Di benzylamine) takes place in a two-phase solvent system so that the hydrogen chloride by-product is sequestered in the aqueous phase and thus prevented from protonating the amine and impeding the progress of the reaction.
These conditions are often called Schotten-Baumann reaction conditions and are applicable more generally.
DBZA (Di benzylamine) is useful as a model for the mechanism of interfacial polymerisation of a diamine with a diacid chloride.
DBZA (Di benzylamine) is used in the industrial manufacturer of numerous pharmaceuticals, including alniditan, lacosamide, moxifloxacin, and nebivolol.
DBZA (Di benzylamine) is also used to manufacture the military explosive hexanitrohexaazaisowurtzitane (HNIW) which is superior to older nitroamine high explosives like HMX and RDX, though it is less stable.
Four of the benzyl groups are removed from hexabenzylhexaazaisowurtzitane by hydrogenolysis catalysed by palladium on carbon and the resulting secondary amine groups are acetylated in acetic anhydride.
DBZA (Di benzylamine) is a methylated benzylamine derivative which is chiral; enantiopure forms are obtained by resolving racemates.
DBZA (Di benzylamine)s racemic form is sometimes known as (±)-α-methylbenzylamine.
DBZA (Di benzylamine) imines due to their relatively high basicity.
DBZA (Di benzylamine) is a colorless to light yellow liquid with a strong odor of ammonia.
DBZA (Di benzylamine) is a primary amine compound having benzyl as the N-substituent.
DBZA (Di benzylamine) has been isolated from Moringa oleifera.
DBZA (Di benzylamine) has a role as a plant metabolite and an allergen.
DBZA (Di benzylamine) is a primary amine and an aralkylamine.
DBZA (Di benzylamine) is a conjugate base of a benzylaminium.
DBZA (Di benzylamine) undergoes oxidative deamination reaction catalyzed by benzylamine oxidase and monoamine oxidase type B.
DBZA (Di benzylamine) is an aromatic amine widely used for the production of organic fine chemicals and many pharmaceutical compounds.
DBZA (Di benzylamine) can be prepared by the hydrogenation of benzonitrile and reductive amination of benzaldehyde using a metal catalyst.
DBZA (Di benzylamine) is a primary alkyl amine.
DBZA (Di benzylamine) is a versatile intermediate and building block in a variety of applications.
DBZA (Di benzylamine) is also used within the coatings industry e.g. as a building block for additives and solvents.
DBZA (Di benzylamine) is both a valuable intermediate for various applications and a building block for chemical synthesis like for the production of Active Pharma Ingredients (APIs) and crop protection agents.
DBZA (Di benzylamine) is a valuable intermediate for various applications and a building block for chemical synthesis used in pharmaceuticals and crop protection agents.
DBZA (Di benzylamine) finds application in the coating industry.
DBZA (Di benzylamine) is involved as a carrier electrolyte for separation of alkali, alkaline earth and ammonium cations in water samples by capillary electrophoresis with indirect UV detection.
DBZA (Di benzylamine) is also used in synthesis of cross-linked porous copolymer supports based on N-(p-vinylbenzoyl)-2-methylalanine, styrene and divinylbenzene.
DBZA (Di benzylamine) is used in colored dyes.
DBZA (Di benzylamine) is often used for medicinal purposes in topical creams and antifungal solutions as well as in vitamins.
DBZA (Di benzylamine) is an organic compound colorless liquid with strong odor of ammonia.
DBZA (Di benzylamine) is also found in apple.
DBZA (Di benzylamine) consists of benzyl group attached to an amine functional group.
DBZA (Di benzylamine) is a common precursor in organic synthesis.
DBZA (Di benzylamine) is found in a plant called Moringa oleifera, which is used to treat diabetes in traditional medicine.
DBZA (Di benzylamine) has the boiling point of 185°C.
DBZA (Di benzylamine) can be produced by reaction between benzyl chloride and ammonia.
DBZA (Di benzylamine) has strong alkaline properties.
DBZA (Di benzylamine) is totally soluble in water.
DBZA (Di benzylamine) is miscible in ethanol, diethyl ether, and acetone.
DBZA (Di benzylamine) is a masked source of ammonia.
DBZA (Di benzylamine) is also called as N-benzylamine, monobenzylamine, benzene methanamine, phenyl methylamine, or aminotoluene.
DBZA (Di benzylamine) is considered a versatile intermediate for a variety of applications.
DBZA (Di benzylamine) and its derivatives are used as chemical intermediates in the production of textile auxiliaries, agrochemicals, dye stuff, pigments, amino acids, and other organic compounds.
The wide range of applications in various end-user industries such as pharmaceutical, chemical, agrochemicals, paints & coatings, textile, and animal health drives the demand for benzylamine.
DBZA (Di benzylamine) is a commodity chemical used in the synthesis of motion-sickness treatments and anticonvulsants, in dyeing textiles, and as a precursor to the high-energy propellant CL-20.
DBZA (Di benzylamine) is an important industrially used amine, which is readily available by hydrogenation of benzonitrile or amination of benzaldehyde or benzyl chloride.
DBZA (Di benzylamine) also occurs in nature and can be isolated.
DBZA (Di benzylamine) is a colorless liquid of ammonia-like odor, which is miscible with water in all proportion.
DBZA (Di benzylamine) is used in the chemical industry as a starting material for other products or as a corrosion inhibitor.
DBZA (Di benzylamine) is an organic chemical compound with the condensed structural formula C6H5CH2NH2 (sometimes abbreviated as PhCH2NH2 or BnNH2).
DBZA (Di benzylamine) consists of a benzyl group, C6H5CH2, attached to an amine functional group.
DBZA (Di benzylamine) is a common precursor in organic chemistry and used in the industrial production of many pharmaceuticals.
DBZA (Di benzylamine) is used as a chemical intermediate for dyes, pharmaceuticals, and polymers.
DBZA (Di benzylamine) is also employed as a corrosion inhibitor and as a brightener in electroplating baths.
DBZA (Di benzylamine) also finds use in the manufacture of explosives.
DBZA (Di benzylamine) may be used as a derivatization agent to increase the sensitivity of 5-hydroxyindoles, catecholamines and catechols in biological samples prior to their determination using high performance liquid chromatography (HPLC) coupled with fluorescence detection.
APPLICATION:
-DBZA (Di benzylamine) was used in modification of alkanethiol monolayers via amide and ester formation reactions for attachment onto metal electrodes.
-DBZA (Di benzylamine) was used as carrier electrolyte for separation of alkali, alkaline earth and ammonium cations in water samples by capillary electrophoresis with indirect UV detection.
-DBZA (Di benzylamine) was used in synthesis of cross-linked porous copolymer supports based on N-(p-vinylbenzoyl)-2-methylalanine, styrene and divinylbenzene.
PROPERTIES:
-Quality Level: 200
-assay: 97%
-form: liquid
-refractive index: n20/D 1.574 (lit.)
-bp: 300 °C (lit.)
-mp: −26 °C (lit.)
-density: 1.026 g/mL at 25 °C (lit.)
-SMILES string: C(NCc1ccccc1)c2ccccc2
-InChI: 1S/C14H15N/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10,15H,11-12H2
-InChI key: BWLUMTFWVZZZND-UHFFFAOYSA-N
SPECIFICATION:
-Color: White to Beige
-Melting Point: 46°C to 55°C
-Boiling Point: 82°C to 84°C (15.0mmHg)
-Flash Point: 78°C
-Assay Percent Range: 94% min. (GC)
-Linear Formula: (CF3)2C6H3CH2NH2
-Packaging: Glass bottle
CHEMICAL IDENTIFIERS:
-Linear Formula: C7H9BF3N
-MDL Number: MFCD01740807
-Pubchem CID: 101841
-IUPAC Name: phenylmethanamine; trifluoroborane
-SMILES: B(F)(F)F.C1=CC=C(C=C1)CN
-InchI Identifier: InChI=1S/C7H9N.BF3/c8-6-7-4-2-1-3-5-7;2-1(3)4/h1-5H,6,8H2;
-InchI Key: YRZFHTRSHNGOSR-UHFFFAOYSA-N
TECHNICAL INFORMATION:
-Physical State: Liquid
-pH: 11.4 at 100 g/l at 20° C
-Storage: Desiccate at room temperature
-Melting Point: 10° C (lit.)
-Boiling Point: 184-185° C (lit.)
-Density: 0.981 g/mL at 25° C
STORAGE:
Desiccate at room temperature.
SYNONYM:
Benzenemethanamine, N-(phenylmethyl)-
N-benzyl-1-phenylmethanamine
N-Benzylbenzylamine
Bibenzylamine
DIBENZYL-AMINE
N,N-Dibenzylamine
(N-Benzylaminomethyl)benzene
UNII-3G0YFX01C6
N-(Phenylmethyl)benzenemethanamine
NSC 4811
3G0YFX01C6
bisbenzylamine
N,N-Dibenylamine
DIBENZYL AMINE
DBA
Accelerator DBA
benzyl benzylamine
Vulcaid 28
EINECS 203-117-7
MFCD00004770
Dibenzylamine, 97%
Bn2NH
AI3-15327
(PhCH2)2NH
NH(CH2Ph)2
