4,4'-Methylenebis(2-chloroaniline)
![]() | |
| Names | |
|---|---|
| IUPAC name
4-[(4-Amino-3-chlorophenyl)methyl]-2-chloroaniline | |
| Other names
•4,4'-Methylene-bis(2-chloroaniline) •Cyanaset •Quodorole •Dacpm •Curalin M •Diamet Kh •Millionate M •Bis amine •MOCA •Bisamine S | |
| Identifiers | |
| 101-14-4 | |
| ChEMBL | ChEMBL82846 |
| ChemSpider | 7262 |
| Jmol interactive 3D | Image |
| KEGG | C10999 |
| PubChem | 7543 |
| |
| |
| Properties | |
| C13H12Cl2N2 | |
| Molar mass | 267.15 g·mol−1 |
| Appearance | Tan-colored pellets or flakes[1] |
| Odor | faint, amine-like[1] |
| Density | 1.44 g/cm3[1] |
| Melting point | 104 to 109 °C (219 to 228 °F; 377 to 382 K)[2] |
| insoluble | |
| Vapor pressure | 0.00001 mmHg (20°C)[1] |
| Hazards | |
| Main hazards | potential occupational carcinogen[1] |
| NFPA 704 | |
| Flash point | 203 °C (397 °F; 476 K) |
| US health exposure limits (NIOSH): | |
| PEL (Permissible) |
none[1] |
| REL (Recommended) |
Ca TWA 0.003 mg/m3 [skin][1] |
| IDLH (Immediate danger |
Ca [N.D.][1] |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| | |
| Infobox references | |
4,4'-Methylenebis(2-chloroaniline) (MOCA, MBOCA, bisamine) is a substance used as a curing agent in polyurethane production.[3] It is a suspected human carcinogen, with a current threshold limit value of 0.01 ppm in the industrial atmosphere. Animal studies have resulted in tumor growth in the liver, lung, and bladder.[1] Employee exposure is often monitored by measurement of urinary MOCA in free and/or conjugated form.[4]
It is a weak base with a slight odor and is reactive to active metals such as sodium, potassium, magnesium and zinc.[1]
References
- 1 2 3 4 5 6 7 8 9 10 "NIOSH Pocket Guide to Chemical Hazards #0411". National Institute for Occupational Safety and Health (NIOSH).
- ↑ "4,4'-Methylenebis(2-chloroaniline)". TCI Chemicals. Retrieved March 17, 2014.
- ↑ RTK HSFS 1250
- ↑ 4,4'-Methylene bis (2-chloroaniline) Health Guideline, Occupational Safety and Health Administration
This article is issued from Wikipedia - version of the Tuesday, December 15, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.

