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111-42-2 - Diethanolamine, 99% - Bis(beta-hydroxyethyl)amine - 2,2'-Iminodiethanol - A13389 - Alfa Aesar

A13389 Diethanolamine, 99%

Numéro CAS
111-42-2
Synonymes
Bis(beta-hydroxyethyl)amine
2,2'-Iminodiethanol

Dimensions Prix ($) Quantité Disponibilité
250g 19,60
500g 26,60
2500g 70,60
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Diethanolamine, 99%

MDL
MFCD00002843
EINECS
203-868-0

Propriétés chimiques

Formule
C4H11NO2
Poids formulaire
105.14
Point de fusion
27-30°
Point d'ébullition
268-270°
Point d'éclair
176°(349°F)
Densité
1.097
Indice de réfraction
1.4770
Sensibilité
Hygroscopic
Solubilité
Miscible with water.

Applications

Diethanolamine is used in the preparation of morpholine and diethanolamides, which is an active ingredient in cosmetics and shampoos. It acts as a surfactant and a corrosion inhibitor. It is utilized to remove hydrogen sulfide and carbon dioxide from natural gas. Further, it is an intermediate used in the rubber chemicals, as a humectant and a softening agent, and as an emulsifier and dispersing agent in agricultural chemicals. In addition to this, it is used in cutting oils, cleaners, soaps, polishers, and pharmaceuticals.

Notes

Hygroscopic and air sensitive. Incompatible with strong oxidizing agents, strong acids, copper, zinc, carbon dioxide and iron.

Références bibliographiques

Boronic acids can be protected as cyclic boronates which are generally high-melting crystalline solids: J. Am. Chem. Soc., 77, 2491 (1955). NMR evidence has been presented indicating that derivatives of this type have a transannular B-N bond: J. Organomet. Chem., 246, 213 (1983):

For use in the modification of a boronic acid cleft in formation of a sodium-saccharide cotransporter, see: J. Org. Chem., 60, 2147 (1995). For use of the butyl cyclic boronate in the formation of a chiral dioxaborolane ligand, see: Org. Synth., 76, 86 (1998). See also Appendix 6.

Hickman, D. A.; Mosner, K.; Ringer, J. W. A continuous diethanolamine dehydrogenation fixed bed catalyst and reactor system. Chem. Eng. J. 2015, 278, 447-453.

Bezgin, F.; Ayaz, N.; Demirelli, K. Synthesis, characterization, and dielectric properties of polymers functionalized with coumarone and diethanolamine. J. Appl. Polym. Sci. 2015, 132 (26), 42164.

Davarpanah, M.; Ahmadpour, A.; Rohani-Bastami, T.; Dabir, H. Synthesis and application of diethanolamine-functionalized polystyrene as a new sorbent for the removal of p-toluenesulfonic acid from aqueous solution. J. Ind. Eng. Chem. 2015, 30, 281-288.

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H302-H315-H318-H351-H373

Harmful if swallowed. Causes skin irritation. Causes serious eye damage. Suspected of causing cancer. May cause damage to organs through prolonged or repeated exposure.

Mentions de prudence: P260u-P201-P280a-P303+P361+P353-P305+P351+P338-P301+P330+P331-P304+P340-P310a-P405-P501a

Obtain special instructions before use. Wear protective gloves and eye/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Merck
14,3107
Beilstein
605315
Code tarifaire harmonisé
2922.12
TSCA
Yes
RTECS
KL2975000

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