GB1031020A - Improvements in or relating to polyurethanes - Google Patents

Info

Publication number

GB1031020A

GB1031020A GB4848163A GB4848163A GB1031020A GB 1031020 A GB1031020 A GB 1031020A GB 4848163 A GB4848163 A GB 4848163A GB 4848163 A GB4848163 A GB 4848163A GB 1031020 A GB1031020 A GB 1031020A

Authority

GB

United Kingdom

Prior art keywords

halogen

polyol

amino

epichlorhydrin

adduct

Prior art date

1963-12-09

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired

Links

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• 229920002635 polyurethane Polymers 0.000 title abstract 2
• 239000004814 polyurethane Substances 0.000 title abstract 2
• 229920005862 polyol Polymers 0.000 abstract 5
• 150000003077 polyols Chemical class 0.000 abstract 5
• 229910052736 halogen Inorganic materials 0.000 abstract 4
• 150000002367 halogens Chemical class 0.000 abstract 4
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
• BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 2
• 125000001691 aryl alkyl amino group Chemical group 0.000 abstract 2
• 125000005843 halogen group Chemical group 0.000 abstract 2
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
• IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 abstract 2
• LBPPDBIHJVJJKN-UHFFFAOYSA-N 1,3,5,7-tetraza-2$l^{5},4$l^{5},6$l^{5},8$l^{5}-tetraphosphacycloocta-1,3,5,7-tetraene-2,2,4,4,6,6,8,8-octamine Chemical compound NP1(N)=NP(N)(N)=NP(N)(N)=NP(N)(N)=N1 LBPPDBIHJVJJKN-UHFFFAOYSA-N 0.000 abstract 1
• VUXWEFDMCHUGCK-UHFFFAOYSA-N 2-n,2-n',4-n,4-n',6-n,6-n',8-n,8-n'-octabutyl-1,3,5,7-tetraza-2$l^{5},4$l^{5},6$l^{5},8$l^{5}-tetraphosphacycloocta-1,3,5,7-tetraene-2,2,4,4,6,6,8,8-octamine Chemical compound CCCCNP1(NCCCC)=NP(NCCCC)(NCCCC)=NP(NCCCC)(NCCCC)=NP(NCCCC)(NCCCC)=N1 VUXWEFDMCHUGCK-UHFFFAOYSA-N 0.000 abstract 1
• GJLDDTXKXLGKHY-UHFFFAOYSA-N 2-n,2-n',4-n,4-n',6-n,6-n'-hexabutyl-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene-2,2,4,4,6,6-hexamine Chemical compound CCCCNP1(NCCCC)=NP(NCCCC)(NCCCC)=NP(NCCCC)(NCCCC)=N1 GJLDDTXKXLGKHY-UHFFFAOYSA-N 0.000 abstract 1
• FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract 1
• 229920005830 Polyurethane Foam Polymers 0.000 abstract 1
• 150000003973 alkyl amines Chemical class 0.000 abstract 1
• 125000003282 alkyl amino group Chemical group 0.000 abstract 1
• 125000002947 alkylene group Chemical group 0.000 abstract 1
• WQJONRMBVKFKOB-UHFFFAOYSA-N cyanatosulfanyl cyanate Chemical compound N#COSOC#N WQJONRMBVKFKOB-UHFFFAOYSA-N 0.000 abstract 1
• 230000009970 fire resistant effect Effects 0.000 abstract 1
• UBIJTWDKTYCPMQ-UHFFFAOYSA-N hexachlorophosphazene Chemical class ClP1(Cl)=NP(Cl)(Cl)=NP(Cl)(Cl)=N1 UBIJTWDKTYCPMQ-UHFFFAOYSA-N 0.000 abstract 1
• 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
• 239000000203 mixture Substances 0.000 abstract 1
• 239000002667 nucleating agent Substances 0.000 abstract 1
• 229920000582 polyisocyanurate Polymers 0.000 abstract 1
• 239000011495 polyisocyanurate Substances 0.000 abstract 1
• 229920001451 polypropylene glycol Polymers 0.000 abstract 1
• 239000011496 polyurethane foam Substances 0.000 abstract 1
• 229920002545 silicone oil Polymers 0.000 abstract 1
• 239000000600 sorbitol Substances 0.000 abstract 1
• -1 sorbitol propylene oxide adducts Chemical class 0.000 abstract 1
• CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 abstract 1
• 229940029284 trichlorofluoromethane Drugs 0.000 abstract 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1

Cited By (3)