Unsymmetrical dimethylhydrazine

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Unsymmetrical dimethylhydrazine
Skeletal formula of unsymmetrical dimethylhydrazine with some implicit hydrogens shown
Ball and stick model of unsymmetrical dimethylhydrazine
Names
Preferred IUPAC name
1,1-Dimethylhydrazine[1]
Other names
Dimazine
Identifiers
3D model (JSmol)
605261
ChEBI
ChemSpider
ECHA InfoCard 100.000.287 Edit this at Wikidata
EC Number
  • 200-316-0
KEGG
MeSH dimazine
RTECS number
  • MV2450000
UNII
UN number 1163
Properties
C2H8N2
Molar mass 60.100 g·mol−1
Appearance Colorless liquid
Odor Ammoniacal, fishy
Density 791 kg m−3 (at 22 °C)
Melting point −57 °C; −71 °F; 216 K
Boiling point 64.0 °C; 147.1 °F; 337.1 K
Miscible[2]
Vapor pressure 13.7 kPa (at 20 °C)
1.4075
Thermochemistry
164.05 J K−1 mol−1
200.25 J K−1 mol−1
Std enthalpy of
formation (ΔfH⦵298)
 48.3 kJ mol−1
Std enthalpy of
combustion (ΔcH⦵298)
 −1982.3 – −1975.1 kJ mol−1
Hazards
Main hazards Carcinogen, spontaneously ignites on contact with oxidizers
GHS pictograms GHS02: Flammable GHS05: Corrosive GHS06: Toxic GHS08: Health hazard GHS09: Environmental hazard
GHS Signal word Danger
GHS hazard statements
 H225, H301, H314, H331, H350, H411
P210, P261, P273, P280, P301+310
NFPA 704 (fire diamond)
4
3
1
Flash point −10 °C (14 °F; 263 K)
248 °C (478 °F; 521 K)
Explosive limits 2–95%
Lethal dose or concentration (LD, LC):
LD50 (median dose)
  • 122 mg kg−1 (oral, rat)
  • 1.06 g kg−1 (dermal, rabbit)
LC50 (median concentration)
  • 252 ppm (rat, 4 hr)
  • 172 ppm (mouse, 4 hr)
  • 392 ppm (hamster, 4 hr)
  • 3580 ppm (dog, 15 min)
  • 1410 ppm (rat, 1 hr)
  • 981 ppm (dog, 1 hr)[3]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 0.5 ppm (1 mg/m3) [skin][2]
REL (Recommended)
 Ca C 0.06 ppm (0.15 mg/m3) [2 hr][2]
IDLH (Immediate danger)
 Ca [15 ppm][2]
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Unsymmetrical dimethylhydrazine (UDMH; 1,1-dimethylhydrazine ; НДМГ) is a chemical compound with the formula H2NN(CH3)2 that is used as a rocket propellant. It is a colorless liquid, with a sharp, fishy, ammonia-like smell typical for organic amines. Samples turn yellowish on exposure to air and absorb oxygen and carbon dioxide. It is miscible with water, ethanol, and kerosene. In concentration between 2.5% and 95% in air, its vapors are flammable. It is not sensitive to shock. Symmetrical dimethylhydrazine, 1,2-dimethylhydrazine is also known but is not as useful.[4]

Production[]

UDMH is produced industrially by two routes.[4] Based on the Olin Raschig process, one method involves reaction of monochloramine with dimethylamine giving 1,1-dimethylhydrazinium chloride:

(CH3)2NH + NH2Cl → (CH3)2NNH2 ⋅ HCl

In the presence of suitable catalysts, acetylhydrazine can be N-dimethylated using formaldehyde and hydrogen to give the N,N-dimethyl-N'-acetylhydrazine, which can subsequently be hydrolyzed:

CH3C(O)NHNH2 + 2CH2O + 2H2 → CH3C(O)NHN(CH3)2 + 2H2O
CH3C(O)NHN(CH3)2 + H2O → CH3COOH + H2NN(CH3)2

Uses[]

UDMH is often used in hypergolic rocket fuels as a bipropellant in combination with the oxidizer nitrogen tetroxide and less frequently with IRFNA (inhibited red fuming nitric acid) or liquid oxygen. UDMH is a derivative of hydrazine and is sometimes referred to as a hydrazine. As a fuel, it is described in specification MIL-PRF-25604 in the United States.[5]

UDMH is stable and can be kept loaded in rocket fuel systems for long periods, which makes it appealing for use in many liquid rocket engines, despite its cost. In some applications, such as the OMS in the Space Shuttle or maneuvering engines, monomethylhydrazine is used instead due to its slightly higher specific impulse. In some kerosene-fueled rockets, UDMH functions as a starter fuel to start combustion and warm the rocket engine prior to switching to kerosene.

UDMH has higher stability than hydrazine, especially at elevated temperatures, and can be used as its replacement or together in a mixture. UDMH is used in many European, Russian, Indian, and Chinese rocket designs. The Russian SS-11 Sego (aka 8K84) ICBM, SS-19 Stiletto (aka 15A30) ICBM, Proton, Kosmos-3M, R-29RMU2 Layner, R-36M, Rokot (based on 15A30) and the Chinese Long March 2F are the most notable users of UDMH (which is referred to as "heptyl" [codename from Soviet era][citation needed] by Russian engineers[6]). The Titan, GSLV, and Delta rocket families use a mixture of 50% hydrazine and 50% UDMH, called Aerozine 50, in different stages.[7] There is speculation that it is the fuel used in the ballistic missiles that North Korea has developed and tested in 2017.[8]

Safety[]

Hydrazines and its methyl derivatives are toxic but LD50 values have not been reported.[9] It is a precursor to dimethylnitrosamine, which is carcinogenic.[10]

See also[]

References[]

  1. ^ "dimazine - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification. Retrieved 21 February 2012.
  2. ^ Jump up to: a b c d NIOSH Pocket Guide to Chemical Hazards. "#0227". National Institute for Occupational Safety and Health (NIOSH).
  3. ^ "1,1-Dimethylhydrazine". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  4. ^ Jump up to: a b Schirmann, Jean-Pierre; Bourdauducq, Paul (2001). "Hydrazine". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a13_177.
  5. ^ "PERFORMANCE SPECIFICATION PROPELLANT, uns-DIMETHYLHYDRAZINE (MIL-PRF-25604F)". ASSIST Database Quicksearch. 2014-03-11. Retrieved 2020-05-26.
  6. ^ "Following Russian rocket explosion, experts warn of 'major contamination'".
  7. ^ Clark, John D. (1972). Ignition! An Informal History of Liquid Rocket Propellants. Rutgers University Press. p. 45. ISBN 0-8135-0725-1.
  8. ^ Broad, William J.; Sanger, David E. (17 September 2017). "The Rare, Potent Fuel Powering North Korea's Weapons" – via www.nytimes.com.
  9. ^ https://www.fishersci.com/shop/msdsproxy?productName=AC116320100&productDescription=UNSYM-DIMETHYLHYDRAZINE%252C+10ML&catNo=AC116320100&vendorId=VN00032119&storeId=10652
  10. ^ Gangadhar Choudhary, Hugh Hansen (1998). "Human health perspective of environmental exposure to hydrazines: A review". Chemosphere. 37: 801–843. doi:10.1016/S0045-6535(98)00088-5.

External links[]

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