N,N-Diisopropylaminoethanol

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N,N-Diisopropylaminoethanol
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Names
Preferred IUPAC name
2-[Di(propan-2-yl)amino]ethan-1-ol
Other names
2-[Di(propan-2-yl)amino]ethanol
2-(Diisopropylamino)ethanol
Identifiers
3D model (JSmol)
1697955
ChEMBL
ChemSpider
ECHA InfoCard 100.002.307 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 202-536-2
MeSH 2-diisopropylaminoethanol
PubChem CID
RTECS number
  • KK5950000
UNII
UN number 2922
  • InChI=1S/C8H19NO/c1-7(2)9(5-6-10)8(3)4/h7-8,10H,5-6H2,1-4H3 Yes check.svgY
    Key: ZYWUVGFIXPNBDL-UHFFFAOYSA-N Yes check.svgY
  • CC(C)N(CCO)C(C)C
Properties
C8H19NO
Molar mass 145.246 g·mol−1
AppearanceColorless liquid
Odor Ammoniacal
Density 826 mg mL−1
Melting point −39.2 °C; −38.6 °F; 233.9 K
Boiling point 190.1 °C; 374.1 °F; 463.2 K
log P 1.476
Vapor pressure <100 Pa (at 20 °C)
1.442
Hazards
GHS labelling:
GHS-pictogram-acid.svg GHS-pictogram-skull.svg
H302, H311, H314, H331
P261, P280, P305+P351+P338, P310
NFPA 704 (fire diamond)
2
1
1
Flash point 64 °C (147 °F; 337 K)
Lethal dose or concentration (LD, LC):
  • 394 mg kg−1(dermal, rabbit)
  • 860 mg kg−1(oral, rat)
Safety data sheet (SDS) [1]
Related compounds
Related alkanols
Related compounds
Diethylhydroxylamine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

N,N-Diisopropylaminoethanol (DIPA) is a processor for production of various chemicals and also an intermediate in the production of the nerve agents VX and NX. [2] It is a colorless liquid, although aged samples can appear yellow.

Health effects

Inhalation and skin contact are expected to be the primary ways of occupational exposure to this chemical. Based on single exposure animal tests, it is considered to be slightly toxic if swallowed or inhaled, moderately toxic if absorbed through skin as well as being corrosive to eyes and skin. [1] Vapor may be irritating to the eyes and upper respiratory tract. Temporary and reversible visual disturbances characterized by mildly blurred vision, a blue-gray discolorization of sight (blue haze) or halo vision (appearance of a halo when looking at light sources) may also occur.[ citation needed ]

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Lewisite 2 Chemical compound

Lewisite 2(L-2) is an organoarsenic chemical weapon with the formula AsCl(CH=CHCl)2. It is similar to lewisite 1 and lewisite 3 and was first synthesized in 1904 by Julius Arthur Nieuwland. It is usually found as a mixture of 2-chlorovinylarsonous dichloride (lewisite 1) as well as bis(2-chloroethenyl) arsinous chloride (lewisite 2) and tris(2-chlorovinyl)arsine (lewisite 3). Pure lewisite 1 is an oily, colorless liquid, however, the impure mixture can appear amber to black with an odor distinct to geraniums.

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References

  1. 1 2 "SAFETY DATA SHEET 2--(Diisopropylamino)ethanol". SigmaAldrich. MilliporeSigma. November 14, 2021. Retrieved April 27, 2022.{{cite web}}: CS1 maint: url-status (link)
  2. Suzuki, Osamu; Kanako Watanabe, eds. (2005). Drugs and poisons in humans : a handbook of practical analysis (1. Aufl. ed.). Berlin [u.a.]: Springer. pp. 69–90. doi:10.1007/3-540-27579-7_9. ISBN   978-3-540-22277-4.