| 词条 | 1,3-Diaminopropane |
| 释义 |
| Watchedfields = changed | verifiedrevid = 477205113 | ImageFile = 1,3-Diaminopropane.svg | ImageFile_Ref = {{chemboximage|correct|??}} | ImageSize = 160 | ImageName = Skeletal formula of 1,3-diaminopropane | IUPACName = Propane-1,3-diamine | OtherNames = {{Unbulleted list|Propandiamine|1,3-Propylenediamine|Trimethylenediamine|3-Aminopropylamine }} |Section1={{Chembox Identifiers | CASNo = 109-76-2 | CASNo_Ref = {{cascite|correct|CAS}} | PubChem = 428 | ChemSpiderID = 415 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | EINECS = 203-702-7 | UNNumber = 2922 | KEGG = C00986 | KEGG_Ref = {{keggcite|correct|kegg}} | MeSHName = trimethylenediamine | ChEBI = 15725 | ChEBI_Ref = {{ebicite|correct|EBI}} | ChEMBL = 174324 | ChEMBL_Ref = {{ebicite|correct|EBI}} | RTECS = TX6825000 | Beilstein = 605277 | Gmelin = 1298 | 3DMet = B00214 | SMILES = NCCCN | StdInChI = 1S/C3H10N2/c4-2-1-3-5/h1-5H2 | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = XFNJVJPLKCPIBV-UHFFFAOYSA-N | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} }} |Section2={{Chembox Properties | C=3 | H=10 | N=2 | Appearance = Colourless liquid | Odor = Fishy, ammoniacal | Density = 0.888 g mL−1 | MeltingPtK = 261.15 | BoilingPtK = 413.2 | LogP = −1.4 | VaporPressure = <1.1 kPa or 11.5 mm Hg(at 20 °C) | RefractIndex = 1.458 | MagSus = -58.1·10−6 cm3/mol }} |Section3={{Chembox Hazards | GHSPictograms = {{GHS flame}} {{GHS corrosion}} {{GHS skull and crossbones}} | GHSSignalWord = DANGER | HPhrases = {{H-phrases|226|302|310|314}} | PPhrases = {{P-phrases|280|302+350|305+351+338|310}} | NFPA-H = 3 | NFPA-F = 3 | NFPA-R = 0 | FlashPtC = 51 | AutoignitionPtC = 350 | ExploLimits = 2.8–15.2% | LD50 = {{Unbulleted list|177 mg kg−1 (dermal, rabbit)|700 mg kg−1 (oral, rat)}} }} |Section4={{Chembox Related | OtherFunction_label = alkanamines | OtherFunction = {{Unbulleted list|Ethylamine|Ethylenediamine|Propylamine|Isopropylamine|1,2-Diaminopropane|Isobutylamine|tert-Butylamine|n-Butylamine|sec-Butylamine|Putrescine}} | OtherCompounds = 2-Methyl-2-nitrosopropane }} }}1,3-Diaminopropane, also known as {{Not a typo|trimethylenediamine}}, is a simple diamine with the formula (CH2)3(NH2)2. A colourless liquid with a fishy odor, it is soluble in water and many polar organic solvents. It is isomeric with 1,2-diaminopropane. Both are building blocks in the synthesis of heterocycles, such as those used in textile finishing, and coordination complexes. It is prepared by the amination of acrylonitrile followed by hydrogenation of the resulting aminopropionitrile.[1] The potassium salt was used in the alkyne zipper reaction.[2] Known uses of 1,3-Diaminopropane is in the synthesis of piroxantrone and losoxantrone. Safety1,3-Diaminopropane is toxic on skin exposure with an LD50 of 177 mg kg−1 (dermal, rabbit) References1. ^Karsten Eller, Erhard Henkes, Roland Rossbacher, Hartmut Höke "Amines, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. {{DOI|10.1002/14356007.a02_001}} {{Ionotropic glutamate receptor modulators}}{{DEFAULTSORT:Diaminopropane, 1,3-}}2. ^{{cite journal | author = C. A. Brown and A. Yamashita | title = Saline hydrides and superbases in organic reactions. IX. Acetylene zipper. Exceptionally facile contrathermodynamic multipositional isomeriazation of alkynes with potassium 3-aminopropylamide | year = 1975 | journal = J. Am. Chem. Soc. | volume = 97 | issue = 4 | pages = 891–892 | doi = 10.1021/ja00837a034 }} 2 : Diamines|NMDA receptor antagonists |
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