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Phenol, 2,4,6-trinitro-, compd. with N,N-diethylethanamine (1:1) is a chemical compound formed by the combination of 2,4,6-trinitrophenol (TNP) and N,N-diethylethanamine in a 1:1 ratio. TNP, also known as picric acid, is an organic compound with the formula C6H2N3O7 and is a yellow crystalline solid. It is a powerful explosive and was once widely used in military applications. N,N-diethylethanamine, on the other hand, is an organic amine with the formula C6H15N, and it is a colorless liquid with a strong, fishy odor. The combination of these two chemicals results in a new compound with unique properties, which may have potential applications in various fields, such as explosives, chemical synthesis, or pharmaceuticals. However, due to the hazardous nature of both TNP and N,N-diethylethanamine, handling and storage of Phenol, 2,4,6-trinitro-, compd. with N,N-diethylethanamine (1:1) require strict safety measures and precautions.

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900-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 900-50-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,0 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 900-50:
(5*9)+(4*0)+(3*0)+(2*5)+(1*0)=55
55 % 10 = 5
So 900-50-5 is a valid CAS Registry Number.

900-50-5Relevant academic research and scientific papers

Triethylammonium picrate: An above-room-temperature phase transition material to switch quadratic nonlinear optical properties

Asghar, Muhammad Adnan,Zhang, Jing,Han, Shiguo,Sun, Zhihua,Ji, Chengmin,Zeb, Aurang,Luo, Junhua

, p. 285 - 288 (2018)

To switch quadratic nonlinear optical (NLO) effects has become an exciting branch of the NLO material science. However, solid-state molecular crystals showing tunable and switchable NLO behaviors remain scarce. Here, we report an organic picrate-based binary molecular crystal, triethylammonium picrate (TEAP), which undergoes an above-room-temperature phase transition at Tc = 319 K, being solidly confirmed by the thermal and dielectric measurements. A large thermal hysteresis of ~7 K discloses the first-order feature for its phase transition. More strikingly, the quadratic NLO effects of TEAP can be switched in the vicinity of Tc. That is, TEAP exhibits NLO-active response of ~1.5 times as large as that of KDP below Tc (i.e., NLO-on state), while its NLO effects totally disappear above Tc (NLO-off state). Structure analyses disclose that the order-disorder transformations of triethylammonium cations and picrate anions collectively contribute to its phase transition, as well as switchable NLO behaviors. This work opens up a new pathway to the designing and assembling of stimuli-responsive materials.

Design, synthesis and investigations of a series of energetic salts through the variation of amines and concentration of picrate anions

Dharavath, Srinivas,Ghule, Vikas D.,Kumar, Nikhil,Mathpati, Ramling S.,Paul, Avijit Kumar,Tittal, Ram Kumar

, p. 4842 - 4852 (2020/08/17)

Eight new energetic salts combining N-bases (amines) with picrate ions were synthesized in high yields and characterized by NMR (1H and 13C), IR spectroscopy, elemental analysis, and differential thermal analysis. Single-crystal structural studies were pe

Synthesis, structural, spectroscopic and optical studies of charge transfer complex salts

Manikandan, Maruthappan,Mahalingam, Thaiyan,Hayakawa, Yasuhiro,Ravi, Ganesan

, p. 178 - 183 (2013/02/22)

New charge transfer molecular complex adducts of picric acid (C 6H3N3O7) with triethylamine (C 6H15N) and dimethylformamide (HCON(CH3) 2) were synthesized successfully

Infrared Spectroscopic Studies of Hydrogen Bonding in Triethylammonium Slats. Part 4. Rearrangement of Hydrogen-bonded Ion Pairs of Triethylammonium Salts caused by Interaction with Tetrabutylammonium Salts in Solution

Mashkovsky, Alexander A.,Nabiullin, Ahat A.,Odinokov, Stanislav E.

, p. 1879 - 1884 (2007/10/02)

Rearrangement of triethyl- and tetrabutylammonium salts in chloroform solution has been revealed from the characteristic features of the ν(N+H) bands caused by Fermi resonance interaction.Temperature changes of the i.r. spectra show this process to be reversible.Rearrangement constant K1 and K-1 and enthalpies -ΔH (for some cases only) of this process have been determined by measuring the total integrated intensities of the ν(N+H) bands of complexes which are in equilibrium.K1 values of the tetrabutylammonium salts increase with decreasing hydrogen bonding strength in triethylammonium salts.The measured enthalpies of rearrangement and those calculated from the ν(N+H) bands of hydrogen-bonded complexes studied are in agreement.It has also been shown that tetrabutylammonium salts anions can participate in the rearrangement of hydrogen-bonded ion pairs like the organic bases studied previously.

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