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Sodium azide

 
Sci-Tech Dictionary: sodium azide
 
(′sōd·ē·əm ′ā′zīd)

(inorganic chemistry) NaN3 Poisonous, colorless crystals; soluble in water and liquid ammonia; decomposes at 300°C; used in medicine and to make lead azide explosives.


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Wikipedia: Sodium azide
 
Sodium azide
Sodium azide
Other names Sodium trinitride
Smite™
Identifiers
CAS number [26628-22-8]
EC number 247-852-1
UN number 1687
RTECS number VY8050000
Properties
Molecular formula NaN3
Molar mass 65.0099 g/mol
Appearance white solid
Odor odorless
Density 1.846 g/cm3 (20 °C)
Melting point

275 °C decomp.

Solubility in water 41.7 g/100 mL (17 °C)
Solubility in alcohol 0.316 g/100 mL (16 °C)
Solubility in ammonia soluble
Structure
Crystal structure Hexagonal, hR12[1]
Space group R-3m, No. 166
Hazards
MSDS External MSDS
EU Index 011-004-00-7
EU classification Highly toxic (T+)
Dangerous for the environment (N)
R-phrases R28, R32, R50/53
S-phrases (S1/2), S28, S45, S60, S61
NFPA 704
0
4
1
 
Flash point 300 °C
LD50 27 mg/kg (oral, rats/mice)[1]
Related compounds
Other cations Potassium azide
Related compounds Sodium cyanide
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

Sodium azide is the chemical compound with the formula NaN3. This colourless azide salt is a common reagent in organic synthesis, and it is a component in many car airbag systems.

Contents

Structure

Sodium azide is ionic. The N3 group is centrosymmetric with N–N distances of 1.18 Å.[2] Sodium azide is highly soluble in water. Such solutions contain minute amounts of hydrogen azide, as described by the following equilibrium:

N3 + H2O is in equilibrium with HN3 + OH K = 10−4.6

Preparation

The common synthesis method is the "Wislicenus process," which proceeds in two steps from ammonia. In the first step, ammonia is converted to sodium amide:

2 Na + 2 NH3 → 2 NaNH2 + H2

The sodium amide is subsequently combined with nitrous oxide:

2 NaNH2 + N2O → NaN3 + NaOH + NH3

Alternatively the salt can be obtained by the reaction of sodium nitrate with sodium amide.[3]

Applications

Automobile airbags

Sodium azide cannot be melted, but decomposes vigorously to sodium metal and nitrogen gas at approximately 300 °C. The airbag formulations contain mixtures of oxidizers and sodium azide. The formulations are ignited by igniters and accelerants. The igniter is initiated by automobile impact/ deceleration:

2 NaN3 → 2 Na + 3 N2

The sodium that is formed is a potential hazard itself and, in automobile airbags, it is converted by reaction with other ingredients, such as potassium nitrate (KNO3) and silica (SiO2), into an inert alkaline silicate 'glass'.[4]

Organic synthesis

Sodium azide is used in organic synthesis to introduce the azide functional group by displacement of a primary halide. The azide functional group can thereafter be converted to an amine by reduction with either lithium aluminium hydride, a tertiary phosphine such as triphenylphosphine in the Staudinger reaction, or with Raney nickel.

Biochemistry and biomedical uses

Sodium azide is a useful probe reagent, mutagen, and preservative. In hospitals and laboratories, it is a biocide; it is especially important in bulk reagents and stock solutions which may otherwise support bacterial growth where the sodium azide acts as a bacteriostatic by inhibiting cytochrome oxidase in gram-negative bacteria; gram-positive (streptococci, pneumococci, lactobacilli) are resistant[5] (a characteristic similar to antibiotic resistance). It is also used in agriculture (farming) for pest control.

Azide inhibits cytochrome oxidase by binding irreversibly to the heme cofactor in a process similar to the action of carbon monoxide. Sodium azide particularly affects organs that undergo high rates of respiration, such as the heart and the brain.

Reactions

Treatment of sodium azide with strong acids gives the corresponding acid, hydrazoic acid:

H2SO4 + NaN3 → HN3 + NaHSO4

Sodium azide can be destroyed by treatment with nitrous acid solution:[6]

2 NaN3 + 2 HNO2 → 3 N2 + 2 NO + 2 NaOH

Safety

Sodium azide is often compared with cyanide, as poisoned individuals suffer from the same symptoms. Exposure to sodium azide has some or all of the following symptoms within minutes: rapid breathing, restlessness, dizziness, weakness, headache, nausea and vomiting, rapid heart rate, red eyes (gas or dust exposure), clear drainage from the nose (gas or dust exposure), cough (gas or dust exposure), skin burns and blisters (explosion or direct skin contact). Exposure to a large amount of sodium azide may cause these other health effects as well: convulsions, low blood pressure, low heart rate, loss of consciousness, and lung injury, respiratory failure leading to death.[7]

References

  1. ^ a b Stevens E.D., Hope H. (1977). "A Study of the Electron-Density Distribution in Sodium Azide, NaN3". Acta Crystallographica A 33. 
  2. ^ Wells, A.F. (1984), Structural Inorganic Chemistry (5th ed.), Oxford: Clarendon Press, ISBN 0-19-855370-6 
  3. ^ Holleman, A. F.; Wiberg, E. (2001), Inorganic Chemistry, San Diego: Academic Press, ISBN 0-12-352651-5 
  4. ^ Eric A. Betterton (2003). "Environmental Fate of Sodium Azide Derived from Automobile Airbags". Critical Reviews in Environmental Science and Technology 33 (4): 423–458. doi:10.1080/10643380390245002. 
  5. ^ Lichstein, Herman C.; Malcolm H. Soule (1943-06-19). "Studies of the Effect of Sodium Azide on Microbic Growth and Respiration". Journal of Bacteriology 47 (3): 221–230. http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=373901. 
  6. ^ Committee on Prudent Practices for Handling, Storage, and Disposal of Chemicals in Laboratories, Board on Chemical Sciences and Technology, Commission on Physical Sciences, Mathematics, and Applications, National Research Council. (1995). Prudent practices in the laboratory: handling and disposal of chemicals. National Academy Press. ISBN 0309052297. http://books.nap.edu/openbook.php?record_id=4911&page=165. 
  7. ^ Sodium Azide

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