| Identification | Back Directory | [Name]
TRIISOBUTYLAMINE | [CAS]
1116-40-1 | [Synonyms]
TRIISOBUTYLAMINE
Triisobutylamine 98%
tris(2-methylpropyl)amine
tributylamine(non-specificname)
N,N-Diisobutyl-2-methyl-1-propanamine
2-methyl-n,n-bis(2-methylpropyl)-1-propanamin
2-methyl-n,n-bis(2-methylpropyl)-1-propanamine
2-methyl-N,N-bis(2-methylpropyl)propan-1-amine
1-Propanamine, 2-methyl-N,N-bis(2-methylpropyl)- | [EINECS(EC#)]
214-236-9 | [Molecular Formula]
C12H27N | [MDL Number]
MFCD00040501 | [MOL File]
1116-40-1.mol | [Molecular Weight]
185.35 |
| Chemical Properties | Back Directory | [Melting point ]
-21.8°C | [Boiling point ]
192-193 °C770 mm Hg(lit.)
| [density ]
0.766 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.423(lit.)
| [Fp ]
135 °F
| [form ]
clear liquid | [pka]
pK1:10.42(+1) (25°C) | [color ]
Colorless to Almost colorless | [BRN ]
1698950 | [InChI]
1S/C12H27N/c1-10(2)7-13(8-11(3)4)9-12(5)6/h10-12H,7-9H2,1-6H3 | [InChIKey]
IIFFFBSAXDNJHX-UHFFFAOYSA-N | [SMILES]
CC(C)CN(CC(C)C)CC(C)C | [EPA Substance Registry System]
Triisobutylamine (1116-40-1) |
| Hazard Information | Back Directory | [General Description]
Clear pale yellow liquid. | [Air & Water Reactions]
Insoluble in water. | [Reactivity Profile]
TRIISOBUTYLAMINE neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides. | [Health Hazard]
ACUTE/CHRONIC HAZARDS: Toxic. | [Fire Hazard]
TRIISOBUTYLAMINE is combustible. | [Chemical Properties]
Triisobutylamine is flammable. | [Uses]
Triisobutylamine is suitable to develop second generation ionic liquid matrices for MALDI-MS of peptides, proteins and carbohydrates. It may be used in the separation of cis-fatty acid salts and and trans-fatty acid (elaidic acid) salts using a new organic solvent nanofiltration membrane based on polydicyclopentadiene. It may be used as base in the synthesis of acroyl ammonium derivatives. | [Production Methods]
Triisobutylamine is manufactured from isobutanol and
ammonia under heat and pressure. |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Maya High Purity Chemicals
|
| Telephone: |
+86 (573) 82222445 (0)18006601000 452520369 |
| Website: |
www.chemicalbook.com/ShowSupplierProductsList15221/0_EN.htm |
| Company Name: |
Sigma-Aldrich
|
| Telephone: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
| Company Name: |
3A Chemicals
|
| Telephone: |
400-668-9898 |
| Website: |
www.3achem.com |
|