Weight | 74.127 g/mol |
---|---|
Formula | C3H10N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
1,2-DIAMINOPROPANE (78-90-0)
1,2-diaminopropane, (R)-isomer · 1,2-diaminopropane dihydrochloride, (S)-isomer · 1,2-diaminopropane, (S)-isomer
Score:
#1169 in Physics
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#3332 in Chemistry
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- Sigma-Aldrich - 1,2-DIAMINOPROPANE25.60 - 208.50 USD
- Fisher Scientific - Search for 1,2-DIAMINOPROPANE
- TCI - 1,2-DIAMINOPROPANE16.00 - 44.00 USD
- Chiral Cyanide-Bridged MnIIMnIII Ferrimagnets, [MnII(HL)(H2O)][MnIII(CN)6]2H2O (L = S- or R-1,2-diaminopropane): Syntheses, Structures, and Magnetic Behaviors (Journal of the American Chemical Society, 2007)
- Synthesis, Structure, and Magnetic Properties of Mn(salpn)N(3,) a Helical Polymer, and Fe(salpn)N(3), a Ferromagnetically Coupled Dimer (salpnH(2) = N,N'-bis(Salicylidene)-1,3-diaminopropane). (Inorganic Chemistry, 1998)
- The first ferromagnetic tetranuclear nickel(II) complex with a .mu.-azido bridge. Structure and magnetic properties of [Ni4(.mu.-N3)4(2-oxo-1,3-diaminopropane)2(2-hydroxo-1,3-diaminopropane)2](ClO4)2 (Inorganic Chemistry, 1993)
- Identification and analysis of a gene encoding L-2,4-diaminobutyrate:2-ketoglutarate 4-aminotransferase involved in the 1,3-diaminopropane production pathway in Acinetobacter baumannii. (Journal of Bacteriology, 1997)
- Synthesis and spectral studies of 5-[3-(1,2,4-triazolyl-azo]-2,4-dihydroxybenzaldehyde (TA) and its Schiff bases with 1,3-diaminopropane (TAAP) and 1,6-diaminohexane (TAAH). Their analytical application for spectrophotometric microdetermination of cobalt(II). Application in some radiochemical studies (Dyes and Pigments, 2005)
- Synthesis, structure, and magnetic properties of [MnIII(salpn)NCS]n, a helical polymer, and the dimer [MnIII(salpn)NCS]2. Weak ferromagnetism in [MnIII(salpn)NCS]n related to the strong magnetic anisotropy in Jahn-Teller MnIII (salpnH2 = N,N'-bis(salicylidene)-1,3-diaminopropane). (Inorganic Chemistry, 2003)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H226: Flammable liquid and vapor
Warning Flammable liquids - Category 3 - H312: Harmful in contact with skin
Warning Acute toxicity, dermal - Category 4 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - H402: Harmful to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 3 - 1,2-diaminopropane, (R)-isomer
- 1,2-diaminopropane dihydrochloride, (S)-isomer
- 1,2-diaminopropane, (S)-isomer
- 1,2-diaminopropane acetate
- 1,2-diaminopropane diacetate
- 1,2-diaminopropane dihydrochloride, (R)-isomer
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SMILESCC(CN)N
-
InChIKeyAOHJOMMDDJHIJH-UHFFFAOYSA-N
- Pubchem - 1,2-DIAMINOPROPANE
- Wikipedia - 1,2-propanediamine
1,2-Diaminopropane (1,2-propanediamine) is organic compound with the formula CH3CH(NH2)CH2NH2. It is the simplest chiral diamine commonly used as a bidentate ligand in coordination chemistry. The compound is a colorless liquid at room temperature.
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