Names | |
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Other names Barium dinitride | |
Identifiers | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.038.706 |
EC Number |
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PubChem CID | |
UN number | 1687 |
CompTox Dashboard (EPA) | |
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Properties | |
Ba(N3)2 | |
Molar mass | 221.37 g/mol |
Appearance | White crystalline solid |
Odor | Odourless |
Density | 2.936 g/cm3 [1] |
Melting point | 126 °C (259 °F; 399 K) |
Boiling point | 160 °C (320 °F; 433 K) (initial decomposition) [2] >217 °C (deflagrates) 180 °C (initial decomposition), [3] 225 °C explosion |
11.5 g/100 mL (0 °C) 14.98 g/100 mL (15.7 °C) 15.36 g/100 mL (20 °C) 22.73 g/100 mL (52.1 °C) 24.75 g/100 mL (70 °C) [4] | |
Solubility in ethanol | 0.017 g/100 mL (16 °C) [5] |
Solubility in acetone | Insoluble |
Solubility in ether | Insoluble |
Structure | |
Monoclinic | |
Hazards | |
GHS labelling: | |
Danger | |
H200, H301, H315, H319, H331, H335 | |
P210, P240, P264, P280, P305+P351+P338, P310 | |
Safety data sheet (SDS) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Barium azide is an inorganic azide with the formula Ba(N3)2. It is a barium salt of hydrazoic acid. Like most azides, it is explosive. It is less sensitive to mechanical shock than lead azide.
Barium azide may be prepared by reacting sodium azide with a soluble barium salt. Care should be taken to prevent large crystals from forming in the solution as barium azide crystals will explode if subjected to friction/shock or if fully dried. The product should be stored submerged in ethanol.[ citation needed ]
Barium azide can be used to make azides of magnesium, sodium, potassium, lithium, rubidium and zinc with their respective sulfates. [4]
It can also be used as a source for high purity nitrogen by heating:
This reaction liberates metallic barium, which is used as a getter in vacuum applications.
In chemistry, azide is a linear, polyatomic anion with the formula N−3 and structure −N=N+=N−. It is the conjugate base of hydrazoic acid HN3. Organic azides are organic compounds with the formula RN3, containing the azide functional group. The dominant application of azides is as a propellant in air bags.
Sodium azide is an inorganic compound with the formula NaN3. This colorless salt is the gas-forming component in some car airbag systems. It is used for the preparation of other azide compounds. It is an ionic substance, is highly soluble in water, and is very acutely poisonous.
Hydrazoic acid, also known as hydrogen azide or azoimide, is a compound with the chemical formula HN3. It is a colorless, volatile, and explosive liquid at room temperature and pressure. It is a compound of nitrogen and hydrogen, and is therefore a pnictogen hydride. It was first isolated in 1890 by Theodor Curtius. The acid has few applications, but its conjugate base, the azide ion, is useful in specialized processes.
Potassium cyanate is an inorganic compound with the formula KOCN. It is a colourless solid. It is used to prepare many other compounds including useful herbicide. Worldwide production of the potassium and sodium salts was 20,000 tons in 2006.
Silver azide is the chemical compound with the formula AgN3. It is a silver(I) salt of hydrazoic acid. It forms a colorless crystals. Like most azides, it is a primary explosive.
Trimethylsilyl azide is the organosilicon compound with the formula (CH3)3SiN3. A colorless liquid, it is a reagent in organic chemistry, serving as the equivalent of hydrazoic acid.
Ammonium azide is the chemical compound with the formula [NH4]N3, being the salt of ammonia and hydrazoic acid. Like other inorganic azides, this colourless crystalline salt is a powerful explosive, although it has a remarkably low sensitivity. [NH4]N3 is physiologically active and inhalation of small amounts causes headaches and palpitations. It was first obtained by Theodor Curtius in 1890, along with other azides.
Potassium azide is the inorganic compound having the formula KN3. It is a white, water-soluble salt. It is used as a reagent in the laboratory.
Lithium azide is the lithium salt of hydrazoic acid. It is an unstable and toxic compound that decomposes into lithium and nitrogen when heated.
Chlorine azide is an inorganic compound that was discovered in 1908 by Friedrich Raschig. Concentrated ClN3 is notoriously unstable and may spontaneously detonate at any temperature.
Silicon tetraazide is a thermally unstable binary compound of silicon and nitrogen with a nitrogen content of 85.7%. This high-energy compound combusts spontaneously and can only be studied in a solution. A further coordination to a six-fold coordinated structure such as a hexaazidosilicate ion [Si(N3)6]2− or as an adduct with bicationic ligands Si(N3)4·L2 will result in relatively stable, crystalline solids that can be handled at room temperature.
Bromine azide is an explosive inorganic compound with the formula BrN3. It has been described as a crystal or a red liquid at room temperature. It is extremely sensitive to small variations in temperature and pressure, with explosions occurring at Δp ≥ 0.05 Torr and also upon crystallization, thus extreme caution must be observed when working with this chemical.
Barium manganate is an inorganic compound with the formula BaMnO4. It is used as an oxidant in organic chemistry. It belongs to a class of compounds known as manganates in which the manganese resides in a +6 oxidation state. Manganate should not to be confused with permanganate which contains manganese(VII). Barium manganate is a powerful oxidant, popular in organic synthesis and can be used in a wide variety of oxidation reactions.
Fluorine azide or triazadienyl fluoride is a yellow green gas composed of nitrogen and fluorine with formula FN3. Its properties resemble those of ClN3, BrN3, and IN3. The bond between the fluorine atom and the nitrogen is very weak, leading to this substance being very unstable and prone to explosion. Calculations show the F–N–N angle to be around 102° with a straight line of 3 nitrogen atoms.
Rubidium azide is an inorganic compound with the formula RbN3. It is the rubidium salt of the hydrazoic acid HN3. Like most azides, it is explosive.
Zinc azideZn(N3)2 is an inorganic compound composed of zinc cations (Zn2+) and azide anions (N−3). It is a white, explosive solid that can be prepared by the protonolysis of diethylzinc with hydrazoic acid:
Iodine azide is an explosive inorganic compound, which in ordinary conditions is a yellow solid. Formally, it is an inter-pseudohalogen.
Caesium azide or cesium azide is an inorganic compound of caesium and nitrogen. It is a salt of azide with the formula CsN3.
Boron triazide, also known as triazidoborane, is a thermally unstable compound of boron and nitrogen with a nitrogen content of 92.1 %. Formally, it is the triazido derivative of borane and is a covalent inorganic azide. The high-energy compound, which has the propensity to undergo spontaneous explosive decomposition, was first described in 1954 by Egon Wiberg and Horst Michaud of the University of Munich.
Homoleptic azido compounds are chemical compounds in which the only anion or ligand is the azide group, -N3. The breadth of homoleptic azide compounds spans nearly the entire periodic table. With rare exceptions azido compounds are highly shock sensitive and need to be handled with the upmost caution. Binary azide compounds can take on several different structures including discrete compounds, or one- two, and three-dimensional nets, leading some to dub them as "polyazides". Reactivity studies of azide compounds are relatively limited due to how sensitive they can be. The sensitivity of these compounds tends to be correlated with the amount of ionic or covalent character the azide-element bond has, with ionic character being far more stable than covalent character. Therefore, compounds such as silver or sodium azide – which have strong ionic character – tend to possess more synthetic utility than their covalent counterparts. A few other notable exceptions include polymeric networks which possess unique magnetic properties, group 13 azides which unlike most other azides decompose to nitride compounds (important materials for semiconductors), other limited uses as synthetic reagents for the transfer for azide groups, or interest in high energy density materials.
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