PRODUCTS

TRIALLYLAMINE

EC / List no.: 203-048-2
CAS no.: 102-70-5
Mol. formula: C9H15N

Triallylamine (C9 H15 N) is an organic compound belonging to the unsaturated amines .
The compound can be used for the preparation of other compounds, as a catalyst and as a corrosion inhibitor.

Features
At room temperature, triallylamine is a colorless liquid.
The compound is slightly soluble in water and in many organic solvents such as ethanol , diethyl ether, acetone and benzene .
Triallylamine is a medium strong base and pK a value is 8.31 .

Production and use of
Triallylamine can be prepared by the reaction between allyl chloride and ammonia .
In this reaction, allylamine and diallylamine are further formed .
Triallylamine can be used in the preparation of other organic compounds.
As a catalyst, it can be used in the production of polyesters and butadiene polymers.
In addition, triallylamine can be used as a corrosion inhibitor.

Triallylamine appears as a colorless liquid with a fishlike odor.
Density 0.800 g / cm3 and insoluble in water.
Hence floats on water.
Flash point 103°F.
Vapors heavier than air.
Used to make other chemicals.

Chemical Properties
dark brown liquid
Triallylamine is a flammble liquid.
Triallylamine can be detected at 0.5 ppm and is severely irritating at 75 ppm.

Uses:
Triallylamine is used in organic synthesis.
Triallylamine has been proposed as a catalyst for the production of polyesters and as an initiator for the polymerization of butadiene.

Triallylamine (TAA) reacts with primary aromatic amines in the presence of a ruthenium catalyst to form 2-ethyl-3-methylquinolines.
TAA undergoes hydrozirconation followed by transmetalation with germanium tetrachloride to form 1-aza-5-germa-5-chlorobicyclo[3.3.3]undecane.
This compound can react with Grignard or lithium reagents to form the corresponding 5-organo compounds.
The cycloaddition of TAA to fluorinated 1,3,4-oxadiazoles affords octahydro-2,7-methanofuro[3,2-c]pyridines.

Production Methods
Triallylamine is manufactured using allyl chloride and ammonia under heat and pressure.
Triallylamine is used as a solvent and in organic syntheses.

General Description
A colorless liquid with a fishlike odor.
Density 0.800 g / cm3 and insoluble in water. Hence floats on water.
Flash point 103°F.
Vapors heavier than air.
May irritate skin and eyes.
Used to make other chemicals.

Air & Water Reactions
Flammable.
Insoluble in water.

Triallylamine is used as an intermediate for the manufacture of rubber chemicals, ion exchange resins, polymerization initiators, quaternary ammonium salts, cross-linking agents

A chemical structure of a molecule includes the arrangement of atoms and the chemical bonds that hold the atoms together. The TRIALLYLAMINE molecule contains a total of 24 bond(s) There are 9 non-H bond(s), 3 multiple bond(s), 6 rotatable bond(s), 3 double bond(s) and 1 tertiary amine(s) (aliphatic).

The carbon atoms in the chemical structure of TRIALLYLAMINE are implied to be located at the corner(s) and hydrogen atoms attached to carbon atoms are not indicated – each carbon atom is considered to be associated with enough hydrogen atoms to provide the carbon atom with four bonds.

Triallylamine is used in organic synthesis and resin modification.

Triallylamine is used as crosslinking agent of high absorbent and intermediate of ion-exchange resin.

Triallylamine is reported that Triallylamine can be used as a catalyst for the production of polyester and an initiator of butadiene polymerization

CAS No.: 102-70-5
Name: 2-Propen-1-amine,N,N-di-2-propen-1-yl-
Superlist Name: Triallylamine
Formula: C9H15N
Synonyms: 2-Propen-1-amine,N,N-di-2-propenyl- (9CI);Triallylamine (6CI,7CI,8CI);N,N-Di-2-propenyl-2-propen-1-amine;Tris(2-propenyl)amine;
Molecular Weight: 137.22
EINECS: 203-048-2
CAS No.: 102-70-5
Melting Point: -70 °C
Boiling Point: 157.6 °C at 760 mmHg
Flash Point: 30.6 °C
Appearance: dark brown liquid
Risk Codes: 10-20/21/22-34
Safety: 16-26-36/37/39-45
Transport Information: UN 2610 3/PG 3
Assay: 99PCT MIN,GC

Triallylamine uses and applications include: unsaturated polyester resin comonomer; crosslinking comonomer; production of some rubbers, ion exchange resins, organic chemicals

Property
Triallylamine is transparent and colorless to yellowish liquid, has ammoniac odor.
Relative density(water=1):0.809g/cm³ melting point:-70℃, boiling point:155-156℃, flash point:39.4℃.

Use
Triallylamine is mainly applied in organic synthesis and resin modifier, also can be used in the crosslinking of high absorbent and the intermediates of ion exchange resin.
According to some reports, it can be used in producing polyester activator and the evocating agent of butadiene polymerization.

Specification :
Colourless and transparent liquid with yellow
Product description :
Colourless and transparent liquid with yellow purity>98%
Uses :
Organic synthesis, Pharmaceutical Intermediates

Triallylamine is transparent and colorless to yellowish liquid, has ammoni

Appearance and properties: dark brown liquid
Density: 0.79 g/mL at 25 °C(lit.)
Boiling point: 150-151 °C(lit.)
Melting point: -70°C Flash point: 87 °F
Refractive index: n20/D 1.451(lit.)
Water solubility: 250 g/100 mL

Stability: Stable. Flammable. Incompatible with strong oxidizing agents.

Storage conditions:
The warehouse is ventilated, low temperature and dry, and stored separately from oxidants, food additives, and acids

Uses:
Used in organic synthesis and resin modification, also used as a cross-linking agent for superabsorbents, intermediates of ion exchange resins.

Triallylamine is mainly applied in organic synthesis and resin modifier, also can be used in the crosslinking of high absorbent and the intermediates of ion exchange resin.
According to some reports, it can be used in producing polyester activator and the evocating agent of butadiene polymerization.

organic material, the monomer of polymers, pharmaceutical intermediate and modified agent for resin

About Triallylamine
Helpful information
Triallylamine is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, for intermediate use only.

Consumer Uses
ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which Triallylamine is most likely to be released to the environment.

Article service life
ECHA has no public registered data on the routes by which Triallylamine is most likely to be released to the environment.
ECHA has no public registered data indicating whether or into which articles the substance might have been processed.

Widespread uses by professional workers
ECHA has no public registered data indicating whether or in which chemical products the substance might be used.
ECHA has no public registered data on the types of manufacture using Triallylamine. ECHA has no public registered data on the routes by which Triallylamine is most likely to be released to the environment.

Formulation or re-packing
ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which Triallylamine is most likely to be released to the environment.

Uses at industrial sites
ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the types of manufacture using Triallylamine.
ECHA has no public registered data on the routes by which Triallylamine is most likely to be released to the environment.

Manufacture
ECHA has no public registered data on the routes by which Triallylamine is most likely to be released to the environment.

IUPAC names
N,N-bis(prop-2-enyl)prop-2-en-1-amine
N,N-di(prop-2-enyl)prop-2-en-1-amine
N,N-Di-2-propenyl-2-propen-1-amin
N,N-diallylprop-2-en-1-amine
TriallylaminE
triallylaminetris(prop-2-en-1-yl)amine

SYNONYMS:
TRIALLYLAMINE
102-70-5
2-Propen-1-amine, N,N-di-2-propenyl-
Tris(2-propenyl)amine
N,N-bis(prop-2-enyl)prop-2-en-1-amine
UNII-B6N19XC04R
tris(prop-2-en-1-yl)amine
B6N19XC04R
4-04-00-01061 (Beilstein Handbook Reference)
MFCD00026093
2-Propen-1-amine, N,N-di-2-propen-1-yl-
Triallyl Amine
CCRIS 4876
N,N-diallylprop-2-en-1-amine
HSDB 2904
EINECS 203-048-2
NSC 32635
UN2610
N,N-Di-2-propenyl-2-propen-1-amine
BRN 1740881
triallyl-amine
(CH2=CHCH2)3N
AI3-52705
Triallylamine, 99%
ACMC-1BZCI
DSSTox_CID_6174
DSSTox_RID_78046
DSSTox_GSID_26174
SCHEMBL20656
CHEMBL3188834
DTXSID5026174
N,N-Diallyl-2-propen-1-amine #
ADAL1243817
AMY22241
NSC32635
ZINC1665016
Tox21_300670
ANW-14735
NSC-32635
2-Propen-1-amine,N-di-2-propenyl-
WLN: 1U2N2U1 & 2U1
AKOS015840489
UN 2610
NCGC00248135-01
NCGC00254578-01
CAS-102-70-5
I780
LS-13670
N,N-bis(prop-2-enyl)-2-propen-1-amine
FT-0653420
Triallylamine [UN2610] [Flammable liquid]
A800604
J-000772
Q23779745
2-Propen-1-amine, N,N-di-2-propen-1-yl-, homopolymer
28182-47-0
2-Propen-1-amine, N,N-di-2-propen-1-yl-
AMINOTRI-2-PROPENE
(CH2=CHCH2)3N
n,n-di-2-propenyl-2-propen-1-amin
N,N-Diallyl-2-propen-1-amine
tertiaryamine
Tris(2-propenyl)amine
TRIALLYLAMINE: 97.5%
TRIALLYAMINE HCL
Tri(prop-1-enyl)amine
Trialkylamine
2-Propen-1-amine, N,N-di-2-propenyl-
N，N-Di-2-propenyl-2-propen-1-Amine
TAA
TRIALLYLAMINE
tri-2-propenylamine
1,1',1''-Nitrilotri(2-propene)
N,N-di(prop-2-enyl)prop-2-en-1-amine
tris(prop-2-en-1-yl)aMine
triallylaMate
Triallylamine 99%
Triallylamine >
Triallylamine ISO 9001：2015 REACH