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Not to be confused with [[trans-1,2-Diaminocyclohexane]]

'''1,2-Cyclohexanediamine''' is an organic compound and is chemically a cycloaliphatic amine. It has the [[CAS Registry number]] of 694-83-7. It is a corrosive liquid.<ref>{{Cite web|url=https://pubchem.ncbi.nlm.nih.gov/compound/4610|title=1,2-Cyclohexanediamine|last=PubChem|website=pubchem.ncbi.nlm.nih.gov|language=en|access-date=2020-04-13}}</ref>. This is the [[racemic mixture]] and not the same as [[trans-1,2-Diaminocyclohexane]]. It is often called DCH-99 and also DACH.
'''1,2-Cyclohexanediamine''' is an organic compound and is chemically a cycloaliphatic amine. It has the [[CAS Registry number]] of 694-83-7. It is a corrosive liquid.<ref>{{Cite web|url=https://pubchem.ncbi.nlm.nih.gov/compound/4610|title=1,2-Cyclohexanediamine|last=PubChem|website=pubchem.ncbi.nlm.nih.gov|language=en|access-date=2020-04-13}}</ref>. This is the [[racemic mixture]] and not the same as [[trans-1,2-Diaminocyclohexane]]. It is often called DCH-99 and also DACH.


Revision as of 13:16, 14 April 2020

1,2-Diaminocyclohexane
Names
IUPAC name
cyclohexane-1,2-diamine
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.010.707 Edit this at Wikidata
EC Number
  • 211-776-7
UN number 2735
  • InChI=1S/C6H14N2/c7-5-3-1-2-4-6(5)8/h5-6H,1-4,7-8H2
    Key: SSJXIUAHEKJCMH-UHFFFAOYSA-N
  • C1CCC(C(C1)N)N
Properties
C6H14N2
Molar mass 114.192 g·mol−1
Hazards
GHS labelling:
GHS05: CorrosiveGHS07: Exclamation mark
Danger
H302, H312, H314, H317, H332, H335
P260, P261, P264, P270, P271, P272, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P333+P313, P363, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Not to be confused with trans-1,2-Diaminocyclohexane

1,2-Cyclohexanediamine is an organic compound and is chemically a cycloaliphatic amine. It has the CAS Registry number of 694-83-7. It is a corrosive liquid.[1]. This is the racemic mixture and not the same as trans-1,2-Diaminocyclohexane. It is often called DCH-99 and also DACH.

Manufacture

The product is available commercially as Dytek DCH-99. It maybe manufactured by the hydrogenation of o-phenylenediamine[2].

Uses

The product is used in the production of epoxy curing agents for use in Coatings, Adhesives, Sealants and Elastomers - CASE[3]. It may also be reacted with diethyl maleate utilizing the Michael reaction to produce a polyaspartic compound[4] of CAS number 481040-92-0. It may also be used in lubricants[5]. The poroduct is also advertised as being useful as a chelating agent in a variety of applications including oil production[6].

See also

References

  1. ^ PubChem. "1,2-Cyclohexanediamine". pubchem.ncbi.nlm.nih.gov. Retrieved 2020-04-13.
  2. ^ Kouklovsky, Cyrille; Langlois, Yves; Aguilar, Enrique; Fernández‐García, Jesús M.; Sikervar, Vikas (2014), "(1S,2S)-1,2-Diaminocyclohexane", Encyclopedia of Reagents for Organic Synthesis, American Cancer Society, pp. 1–23, doi:10.1002/047084289x.rn00145.pub3, ISBN 978-0-470-84289-8, retrieved 2020-04-13
  3. ^ "Dytek® DCH-99 by INVISTA - Paint & Coatings". www.ulprospector.com. Retrieved 2020-04-13.
  4. ^ "Dytek® DCH-99 | 1,2-Diaminocyclohexane". Dytek. Retrieved 2020-04-13.
  5. ^ "US Patent for Non-aromatic based antioxidants for lubricants Patent (Patent # 9,273,266 issued March 1, 2016) - Justia Patents Search". patents.justia.com. Retrieved 2020-04-13.
  6. ^ "Technical Data Sheet Dytek DCH 99" (PDF).{{cite web}}: CS1 maint: url-status (link)
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