Monochloramine

Monochloramine
Stereo, skeletal formula of chloramine with all explicit hydrogens added
Spacefill model of chloramine
Names
Other names
  • Chloramine
  • Chloramide[1]
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.031.095 Edit this at Wikidata
EC Number
  • 234-217-9
KEGG
MeSH chloramine
UNII
UN number 3093
  • InChI=1S/ClH2N/c1-2/h2H2 ☒N
    Key: QDHHCQZDFGDHMP-UHFFFAOYSA-N ☒N
  • NCl
Properties
NH
2
Cl
Molar mass 51.476 g mol−1
Appearance Colorless gas
Melting point −66 °C (−87 °F; 207 K)
Acidity (pKa) 14
Basicity (pKb) 15
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Corrosive acid
Ingestion hazards
Corrosive; nausea and vomiting
Inhalation hazards
Corrosive
Eye hazards
Irritation
Skin hazards
Irritation
GHS labelling:
GHS07: Exclamation mark GHS08: Health hazard GHS05: Corrosive
Danger
H290, H314, H315, H319, H335, H372, H412
P234, P260, P261, P264, P270, P271, P273, P280, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P314, P321, P332+P313, P337+P313, P362, P363, P390, P403+P233, P404, P405, P501
NFPA 704 (fire diamond)
Lethal dose or concentration (LD, LC):
935 mg/kg (rat, oral)[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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Monochloramine, often called chloramine, is the chemical compound with the formula NH2Cl. Together with dichloramine (NHCl2) and nitrogen trichloride (NCl3), it is one of the three chloramines of ammonia.[3] It is a colorless liquid at its melting point of −66 °C (−87 °F), but it is usually handled as a dilute aqueous solution, in which form it is sometimes used as a disinfectant. Chloramine is too unstable to have its boiling point measured.[4]

  1. ^ "CHLORAMINE". CAMEO Chemicals. NOAA.
  2. ^ a b "Chloramine T Trihydrate SDS". Fisher.[permanent dead link]
  3. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  4. ^ Lawrence, Stephen A. (2004). Amines: Synthesis, Properties and Applications. Cambridge University Press. p. 172. ISBN 9780521782845.