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| IMINOBISPROPYLAMINE | ||
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PRODUCT IDENTIFICATION |
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| CAS NO. | 56-18-8 |
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| EINECS NO. |
200-261-2 | |
| FORMULA | HN[(CH2)3NH2]2 | |
| MOL WT. | 131.22 | |
| H.S. CODE | 2921.29 | |
| TOXICITY | Oral rat LD50: 738 mg/kg | |
| SYNONYMS | Bis(3-aminopropyl) Amine; 3,3'-Diaminodipropylamine; | |
| 4-Azaheptamethylenediamine; N-(3-aminopropyl)-1,3-Propanediamine; 3,3'-Iminopropylamine; Aminobis(propylamine); Caldine; 3,3'-Diamino Dipropylamine; Imino-bis(3-propylamine); N-(3-Aminopropyl)-1,3-propanediamine; N-3-Aminopropyl-1,3-diaminopropane; 3,3'-iminobispopylamine; 1,7-Diamino-4-Azaheptane; 4-Azaheptane-1,7-diamine; | ||
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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| PHYSICAL STATE | clear liquid | |
| MELTING POINT | -15 C | |
| BOILING POINT |
235 C | |
| SPECIFIC GRAVITY | 0.938 | |
| SOLUBILITY IN WATER | miscible | |
| AUTOIGNITION |
280 C | |
| pH | ||
| VAPOR DENSITY | 4.52 | |
| NFPA RATINGS | Health: 3; Flammability: 1; Reactivity: 2 | |
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REFRACTIVE INDEX |
1.4810 | |
| FLASH POINT |
118 C | |
| STABILITY | Stable under ordinary conditions. | |
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APPLICATIONS |
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Imide refers to any compound which contains the divalent radical
"-C(=O)NHC(=O)-". Imide compounds are derived from ammonia or primary amine,
where two hydrogen atoms are replaced by a bivalent acid group or two monovalent
acid groups, resulting in consisting of two carboxylic acid groups (or one
dicarboxylic acid). In other description, Imide is a compound derived from an
acid anhydride by replacing the oxygen with the =NH group. Imides are monomers
to prepare polyimides that contain repeating imide groups. Aromatic polyimides have better resistance to high temperatures and corrosion than linear
polyimides. Frequently, the term of imide refers to the combined forms such as
maleimides, phthalimides, and succinimides which are used as plastic modifiers
to improve heat-resistant, antioxidant and antifoulant properties. They are used
as intermediates for the synthesis of cross-linking agents, pesticides, dyes,
antiseptics and crystalline adducting agents. They are also useful compounds in
the synthesis of primary amines and amino acids for the application in the field
of medicine and biological research. Phthalimide, derived from phthalic anhydride with ammonium hydroxide
by heating, is used
in the synthesis of primary amines and amino acids. It is used to make synthetic indigo
and phthalocyanine pigments which have macrocyclic structure
showing striking coloring features like porphyrins (biopigments). The radical "=NH" is called imido group. Imido is a prefix
used to denote the presence in a compound of the bivalent group "=NH" attached
to only acid radicals. Imine is a compound containing the bivalent "=NH" group
combined with a bivalent nonacid group, as "R-HC=NH". It is produced by the
condensation reactions of aldehydes or ketones with ammonia (or amines). Imino
is a prefix denoting the presence of the bivalent group "=NH" attached to
nonacid radicals.
3,3'-Iminobispopylamine, aliphatic oligoamine, is used as a polymer cross linkage agent, polyurethane extender and spray coatings. It is used as a chemical intermediate for epoxy curing agents, pharmaceuticals, agrochemicals, and other organic chemicals (e.g auxiliary for the paper, textile, and leather industries) |
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| SALES SPECIFICATION | ||
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APPEARANCE |
clear to yellow liquid | |
| ASSAY (G.C) |
99.0% min | |
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COLOR (APHA) |
20 max | |
| MOISTURE (K.F) | 0.5% max | |
| TRANSPORTATION | ||
| PACKING | 180kgs in Drum | |
| HAZARD CLASS | 8 (Packing Group: III) | |
| UN NO. | 2269 | |
| OTHER INFORMATION | ||
| Hazard Symbols: T C, Risk Phrases: 22-24-26-35-43, Safety Phrases: 26-28-36/37/39-45 | ||
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