2,2,6,6-Tetramethylpiperidine
768-66-1CC1(C)CCCC(C)(C)N1RKMGAJGJIURJSJ-UHFFFAOYSA-N768-66-1DTXSID0061113CHEMBL2448812안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.
Danger
H226 (97.1%): Flammable liquid and vapor [Warning Flammable liquids]
P210, P233, P240, P241, P242, P243, P260, P261, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P303+P361+P353, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P363, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 102 reports by companies from 23 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Chemical: Piperidine, 2,2,6,6-tetramethyl-
REACH registered substance: 2,2,6,6-tetramethylpiperidine (EC: 212-199-3)
2,2,6,6-Tetramethylpiperidine: Does not have an individual approval but may be used under an appropriate group standard
Rats demonstrated effects possibly indicative of neurotoxicity in all test groups of acute inhalation study and high dose group (500 mg/kg) of acute oral study; [EPA - TSCATS] A skin and strong eye irritant; Toxic by ingestion; [Sigma-Aldrich MSDS] See Piperidine.
용도권장되는 용도 실험실용 화학물질.
용도2,2,6,6-Tetramethylpiperidine is used in the syntheses of HMP-Y1, Hibarimicinone and HMP-P1, tyrosine kinase inhibitors.
Many routes for the synthesis of TMP have been reported. One method starts with a conjugate addition reaction of ammonia to phorone. The intermediate triacetone amine is then reduced in a Wolff-Kishner reaction.
불러오는 중…
clear colorless to light yellow-green liquid