Dibutylhexamethylenediamine See also References Navigation menu4835-11-4Interactive image19729100.023.106N,N'-dibutyl-1,6-hexanediamine20972846A8RML53DTXSID60388236539732expanding ite
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chemical compoundpolymersextremely hazardous substanceU.S. Emergency Planning and Community Right-to-Know Act
Dibutylhexamethylenediamine
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Names | |
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Preferred IUPAC name N,N′-Dibutyl-1,6-hexanediamine | |
Other names
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Identifiers | |
CAS Number |
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3D model (JSmol) |
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ChemSpider |
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ECHA InfoCard | 100.023.106 |
EC Number | 225-417-7 |
MeSH | N,N'-dibutyl-1,6-hexanediamine |
PubChem CID |
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RTECS number | MO1250000 |
UNII |
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UN number | 2735 |
CompTox Dashboard (EPA) |
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InChI
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SMILES
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Properties | |
Chemical formula | C14H32N2 |
Molar mass | 228.424 g·mol−1 |
Appearance | Colourless liquid |
Density | 821 mg mL−1 |
Boiling point | 131 to 133 °C (268 to 271 °F; 404 to 406 K) at 4 hPa |
Refractive index (nD) | 1.451 |
Hazards | |
GHS pictograms | |
GHS signal word | DANGER |
GHS hazard statements | H314, H330 |
GHS precautionary statements | P260, P280, P284, P305+351+338, P310 |
Flash point | 113 °C (235 °F; 386 K) |
Related compounds | |
Related compounds |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
N,N’-Dibutylhexamethylenediamine (dibutylhexanediamine) is a chemical compound used in the production of polymers. It is highly toxic upon inhalation,[1] and is listed as an extremely hazardous substance as defined by the U.S. Emergency Planning and Community Right-to-Know Act.
See also
- Hexamethylenediamine
References
^ Kennedy Jr, GL; Chen, HC (1984). "Inhalation toxicity of dibutylhexamethylenediamine in rats". Food and Chemical Toxicology. 22 (6): 425–9. PMID 6539732..mw-parser-output cite.citationfont-style:inherit.mw-parser-output .citation qquotes:"""""""'""'".mw-parser-output .citation .cs1-lock-free abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .citation .cs1-lock-subscription abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registrationcolor:#555.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration spanborder-bottom:1px dotted;cursor:help.mw-parser-output .cs1-ws-icon abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center.mw-parser-output code.cs1-codecolor:inherit;background:inherit;border:inherit;padding:inherit.mw-parser-output .cs1-hidden-errordisplay:none;font-size:100%.mw-parser-output .cs1-visible-errorfont-size:100%.mw-parser-output .cs1-maintdisplay:none;color:#33aa33;margin-left:0.3em.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-formatfont-size:95%.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-leftpadding-left:0.2em.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-rightpadding-right:0.2em
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