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Tetrabutylammonium iodide

Names

[ CAS No. ]:
311-28-4

[ Name ]:
Tetrabutylammonium iodide

[Synonym ]:
N,N,N-Tributyl-1-butanaminium iodide
Bu4NI
Tetra-N-butylammoniumjodid
tetrabutyl-ammonium iodide
Tetrabutylammonium iodide
EINECS 206-220-5
MFCD00011636
TBAI
tetra-n-butyl ammonium iodide
n,n,n-tributylbutan-1-aminium iodide
Ammonium,tetrabutyl-,iodide
1-Butanaminium, N,N,N-tributyl-, iodide (1:1)
tetra-butylammonium iodide
Tetra-n-Butylammonium Iodide

Biological Activity

[Description]:

Tetra-n-butylammonium iodide is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.20

[ Melting Point ]:
141-143 °C(lit.)

[ Molecular Formula ]:
C16H36IN

[ Molecular Weight ]:
369.368

[ Flash Point ]:
100ºC

[ Exact Mass ]:
369.189240

[ LogP ]:
2.00760

[ Stability ]:
Stable. Incompatible with strong oxidizing agents. Light-sensitive.

[ Water Solubility ]:
acetonitrile: 0.1 g/mL, clear, colorless

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
BS5450000
CHEMICAL NAME :
Ammonium, tetrabutyl-, iodide
CAS REGISTRY NUMBER :
311-28-4
LAST UPDATED :
199701
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C16-H36-N.I
MOLECULAR WEIGHT :
369.43
WISWESSER LINE NOTATION :
4K4&4&4 &I

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1990 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
85JCAE "Prehled Prumyslove Toxikologie; Organicke Latky," Marhold, J., Prague, Czechoslovakia, Avicenum, 1986 Volume(issue)/page/year: -,489,1986
TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1600 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPMSAE Journal of Pharmaceutical Sciences. (American Pharmaceutical Assoc., 2215 Constitution Ave., NW, Washington, DC 20037) V.50- 1961- Volume(issue)/page/year: 69,327,1980

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R22;R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
BS5450000

[ HS Code ]:
2827600000

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2827600000

Articles

High-turnover hypoiodite catalysis for asymmetric synthesis of tocopherols.

Science 345(6194) , 291-4, (2014)

The diverse biological activities of tocopherols and their analogs have inspired considerable interest in the development of routes for their efficient asymmetric synthesis. Here, we report that chira...

Tandem cyclization of α-cyano α-alkynyl aryl ketones induced by tert-butyl hydroperoxide and tetrabutylammonium iodide.

Org. Lett. 14(23) , 6024-7, (2012)

The radical cascade protocol of the α-cyano α-TMS/aryl-capped alkynyl aryl ketones promoted by tert-butyl hydroperoxide under catalysis with tetrabutylammonium iodide in refluxing benzene has been dev...

RNA editing in eag potassium channels: biophysical consequences of editing a conserved S6 residue.

Channels (Austin.) 6(6) , 443-52, (2012)

RNA editing at four sites in eag, a Drosophila voltage-gated potassium channel, results in the substitution of amino acids into the final protein product that are not encoded by the genome. These site...


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Related Compounds