Chemical Name | Tetrabutylammonium tribromide |
Synonym |
N,N,N,N-Tetrabutylammonium tribromide
{LY} N,N,N,N-Tetrabutylammonium tribromide
{} {LY} N,N,N,N-Tetrabutylammonium tribromide
{} {} {LY} N,N,N,N-Tetrabutylammonium tribromide
{} {} {} {LY} N,N,N,N-Tetrabutylammonium tribromide
{} {} {} {} {LY} N,N,N,N-Tetrabutylammonium tribromide
{} {} {} {} {} {LY} N,N,N,N-Tetrabutylammonium tribromide
{} {} {} {} {} {} {LY} N,N,N,N-Tetrabutylammonium tribromide
{} {} {} {} {} {} {} {LY} N,N,N,N-Tetrabutylammonium tribromide
{} {} {} {} {} {} {} {} {LY} N,N,N,N-Tetrabutylammonium tribromide
{} {} {} {} {} {} {} {} {} {LY} N,N,N,N-Tetrabutylammonium tribromide
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{} {} {} {} {} {} {} {} {} {} {} {LY} N,N,N,N-Tetrabutylammonium tribromide
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MDL Number | MFCD00012110 |
PubChem Substance ID | 2723680 |
Beilstein Registry Number | 4(4)557 |
CAS Number | 38932-80-8 |
EC Number | 250-023-7 |
Reaxys-RN | 3746114 |
Chemical Name Translation | 四丁基三溴化铵 |
LabNetwork Molecule ID | LN00200679 |
InChI | InChI=1S/C16H36N.Br3/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;1-3-2/h5-16H2,1-4H3;/q+1;-1 |
Canonical SMILES | CCCC[N+](CCCC)(CCCC)CCCC.BrBr[Br-] |
WGK Germany | 3 |
GHS Symbol
Precautionary statements | |
- P303+P361+P353+P310+P363
- P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
- P501 Dispose of contents/container to..… 处理内容物/容器.....
- P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P305+P351+P338
- P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
- P301+P330+P331
- P405 Store locked up. 上锁保管。
- P304+P340
- P260 Do not breathe dust/fume/gas/mist/vapours/spray. 不要吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P304+P340+P310
- P305+P351+P338+P310
- P301+P330+P331+P310
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Hazard statements | |
- H315 Causes skin irritation 会刺激皮肤
- H319 Causes serious eye irritation 严重刺激眼睛
- H335 May cause respiratory irritation 可能导致呼吸道刺激
- H314 Causes severe skin burns and eye damage 导致严重的皮肤灼伤和眼睛损伤
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Personal Protective Equipment |
dust mask type N95 (US), Eyeshields, Gloves |
Signal word |
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Safety Statements | |
- S26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 眼睛接触后,立即用大量水冲洗并征求医生意见;
- S36/37/39 Wear suitable protective clothing, gloves and eye/face protection 穿戴适当的防护服、手套和眼睛/面保护;
- S45 In case of accident or if you feel unwell seek medical advice immediately (show the label where possible) 发生事故时或感觉不适时,立即求医(可能时出示标签);
- S36 Wear suitable protective clothing 穿戴适当的防护服;
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Risk Statements | |
- R36/37/38 Irritating to eyes, respiratory system and skin 对眼睛、呼吸系统和皮肤有刺激性
|
Packing Group | III |
UN Number |
1759
UN3261 |
Hazard Codes |
Xi |
Hazard Class | 8 |
Storage condition |
2-8°C
{LY} 2-8°C
{} {LY} 2-8°C
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{ALF} For Hofman rearrangemt of amides to ureas and carbamates, See: Bull. Chem. Soc. Jpn., 61, 1401 (1988).
{ALF} In catalytic amounts promotes dithioacetalization of aldehydes and ketones, and transthioacetalization of 1,3-dioxolanes and dioxanes with ethane- or propanedithiol: Org. Biomol. Chem., 2, 1670 (2004); the cleavage of dithioacetals to the corresponding carbonyl compounds with stoichiometric amounts of the reagent has also been described: Synlett, 785 (2001). Also catalyzes both the protection and deprotection of carbonyl compounds to 1,3-dithiolanes: Tetrahedron. Lett., 43, 2843 (2002), of aldehydes to 1,1-diacyloxy derivatives: Eur. J. Org. Chem., 441 (2005), and alcohols to tetrahydropyranyl (THP) ethers: Tetrahedron Lett., 42, 7679 (2001). In methanol, t-butyldimethylsilyl (TBDMS), THP, and 4,4'-dimethoxytrityl ethers undergo catalytic deprotection. The reaction is chemoselective, permitting, e.g. selective deprotection of primary DMT, TBDMS, and THP ethers in the presence of other ether protecting groups: Org. Lett., 2, 4177 (2000).
{uni_hamburg} Short: III/20b
{ALF} In catalytic amounts promotes dithioacetalization of aldehydes and ketones, and transthioacetalization of 1,3-dioxolanes and dioxanes with ethane- or propanedithiol: Org. Biomol. Chem., 2, 1670 (2004); the cleavage of dithioacetals to the corresponding carbonyl compounds with stoichiometric amounts of the reagent has also been described: Synlett, 785 (2001). Also catalyzes both the protection and deprotection of carbonyl compounds to 1,3-dithiolanes: Tetrahedron. Lett., 43, 2843 (2002), of aldehydes to 1,1-diacyloxy derivatives: Eur. J. Org. Chem., 441
{ALF} Mild brominating agent. Alkenes are converted to vic-dibromides in high yields. In ethylene glycol, ketones can be converted directly to ɑ-bromo ethylene acetals in good yield, providing convenient access to ɑ,ß-unsaturated ketones: Bull. Soc. Chim. Belg., 93, 157 (1984); Synth. Commun., 15, 213 (1985). Aromatic amines and