Substance

ID:716306

Names and Identifiers
IUPAC name
2-[(2-hydroxyethyl)amino]ethan-1-ol
IUPAC Traditional name
diethanolamine
Synonyms
2,2'-Iminodiethanol二乙醇胺DiethanolamineBis(beta-hydroxyethyl)amine
Registration numbers
EC Number
MDL Number
CAS Number
Beilstein Number
Merck Index
Properties
Physical Property
Density
1.097
Melting Point
27-30°C
Boiling Point
268-270°C
Refractive Index
1.4770
Flash Point
176°C(349°F)
Safety Information
GHS Pictograms
GHS05
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS08
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
RTECS
KL2975000
Storage Warning
Hygroscopic
Risk Statements
22-38-41-48/22
European Hazard Symbols
Harmful Harmful (X)
TSCA Listed
GHS Hazard statements
H318-H315-H373-H302
GHS Precautionary statements
P260-P280-P305+P351+P338-P302+P352-P321-P501A
Safety Statements
26-36/37/39-46
Product Information
Purity
99%
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• 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.