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Diethylaminoethanol

Diethylaminoethanol Structure
CAS No.
100-37-8
Chemical Name:
Diethylaminoethanol
Synonyms
DEAE;DEEA;DIETHYLETHANOLAMINE;N,N-DIETHYLETHANOLAMINE;2-DIETHYLAMINOETHANOL;N,N-Diethyl-2-aminoethanol;Dehydasal;Rotec A.O.;Pennad 150;Perdilaton
CBNumber:
CB5752557
Molecular Formula:
C6H15NO
Molecular Weight:
117.19
MOL File:
100-37-8.mol
Modify Date:
2024/4/29 22:41:02

Diethylaminoethanol Properties

Melting point -70 °C
Boiling point 161 °C (lit.)
Density 0.884 g/mL at 25 °C (lit.)
vapor density 4.04 (vs air)
vapor pressure 1 mm Hg ( 20 °C)
refractive index n20/D 1.441(lit.)
Flash point 120 °F
storage temp. Store below +30°C.
solubility soluble
pka 14.74±0.10(Predicted)
form Crystalline Powder
color White to pale yellow
PH Range 10
PH 11.5 (100g/l, H2O, 20℃)
Odor Characteristic ammoniacal odor
explosive limit 0.7%(V)
Water Solubility soluble
FreezingPoint -70℃
Merck 14,3112
BRN 741863
Exposure limits NIOSH REL: TWA 10 ppm (50 mg/m3), IDLH 100 ppm; OSHA PEL: TWA 10 ppm; ACGIH TLV: TWA 2 ppm (adopted).
Stability Stable. Flammable. Incompatible with strong oxidizing agents, acids. Moisture sensitive. Hygroscopic.
InChIKey BFSVOASYOCHEOV-UHFFFAOYSA-N
LogP 0.21 at 23℃
CAS DataBase Reference 100-37-8(CAS DataBase Reference)
NIST Chemistry Reference Ethanol, 2-(diethylamino)-(100-37-8)
EPA Substance Registry System Diethylaminoethanol (100-37-8)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS05,GHS06
Signal word  Danger
Hazard statements  H226-H302-H311+H331-H314
Precautionary statements  P210-P280-P301+P330+P331-P303+P361+P353-P304+P340+P311-P305+P351+P338
Hazard Codes  C
Risk Statements  10-20/21/22-34
Safety Statements  25-26-36/37/39-45
RIDADR  UN 2686 8/PG 2
OEB A
OEL TWA: 10 ppm (50 mg/m3) [skin]
WGK Germany  1
RTECS  KK5075000
Autoignition Temperature 270 °C
TSCA  Yes
HazardClass  8
PackingGroup  II
HS Code  29221985
Toxicity LD50 orally in Rabbit: 1300 mg/kg LD50 dermal Rabbit 1109 mg/kg
IDLA 100 ppm
NFPA 704
2
2 0

Diethylaminoethanol price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 8.03273 2-(Diethylamino)-ethanol for synthesis 100-37-8 1L ₹3429.99 2022-06-14 Buy
Sigma-Aldrich(India) 8.03273 2-(Diethylamino)-ethanol for synthesis 100-37-8 100ML ₹3620 2022-06-14 Buy
Sigma-Aldrich(India) 471321 2-(Diethylamino)ethanol ≥99.5% 100-37-8 100ML ₹3918.65 2022-06-14 Buy
Sigma-Aldrich(India) 8.03273 2-(Diethylamino)-ethanol for synthesis 100-37-8 25L ₹39070 2022-06-14 Buy
Sigma-Aldrich(India) 471321 2-(Diethylamino)ethanol ≥99.5% 100-37-8 500ML ₹5347.55 2022-06-14 Buy
Product number Packaging Price Buy
8.03273 1L ₹3429.99 Buy
8.03273 100ML ₹3620 Buy
471321 100ML ₹3918.65 Buy
8.03273 25L ₹39070 Buy
471321 500ML ₹5347.55 Buy

Diethylaminoethanol Chemical Properties,Uses,Production

Chemical Properties

Colorless liquid with a nauseating, weak, ammonia odor; hygroscopic; very soluble in water; soluble in alcohol, ether acetone, benzene, and petroleum ether.

Physical properties

Colorless, hygroscopic liquid with a nauseating, ammonia-like odor. Experimentally determined detection and recognition odor threshold concentrations were 50 μg/m3 (11 ppbv) and 190 μg/m3 (40 ppbv), respectively (Hellman and Small, 1974).

Uses

Water-soluble salts; textile softeners; antirust formulations; fatty acid derivatives; pharmaceuticals; curing agent for resins; emulsifying agents in acid media; organic synthesis.

Production Methods

2-Diethylaminoethanol (DEAE) is a tertiary amine produced by reaction of ethylene oxide or ethylene chlorhydrin and diethylamine (RTECS 1988). Itokazu (1987) has modified this process for manufacture of DEAE without eventual discoloration. Production in this country exceeds 2866 pounds per year (HSDB 1988).

Definition

ChEBI: 2-diethylaminoethanol is a member of the class of ethanolamines that is aminoethanol in which the hydrogens of the amino group are replaced by ethyl groups. It is a member of ethanolamines, a tertiary amino compound and a primary alcohol. It derives from an ethanolamine. It derives from a hydride of a triethylamine.

General Description

A colorless liquid. Flash point 103-140°F. Less dense than water . Vapors heavier than air. Produces toxic oxides of nitrogen during combustion. Causes burns to the skin, eyes and mucous membranes.

Air & Water Reactions

Flammable. Soluble in water. Diethylaminoethanol is sensitive to moisture. Slowly hydrolyzes.

Reactivity Profile

Diethylaminoethanol is an aminoalcohol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Diethylaminoethanol can react with strong oxidizers and acids.

Health Hazard

INHALATION: Irritation of mucous membranes.
EYES: Corrosive, causes intense pain.
SKIN: Severe irritation. May cause allergic skin reaction.
INGESTION: Gastrointestinal irritation.
Breathing Diethylaminoethanol can irritate the nose, throat and lungs causing coughing, wheezing and/or shortness of breath.

Industrial uses

Diethylaminoethanol(DEAE) is used in the pharmaceutical industry for the manufacture of the local anesthetics procaine and chloroquine; and in the chemical industry for the manufacture of water-soluble salts, fatty-acid derivatives, derivatives containing tertiary amine groups, emulsifiers, special soaps, cosmetics and textiles and fibers (HSDB 1988). It also is used in chromatography in chemistry and biochemistry laboratories (DEAE is useful as an ion-exchange matrix; DEAE-cellulose columns are used for purification of proteins and DNA, and DEAE-silica for phospholipid separations). In other industries DEAE is used in some antirust compositions and in textile softeners (Hawley 1977; HSDB 1988). It is also used widely as a steam additive in large buildings requiring humidifiers.

Safety

There is a lack of data regarding human toxicity of Diethylaminoethanol. The greatest industrial hazard however, is thought to be to the eyes from contact with the fluid, which is comparable in severity to ammonium hydroxide as an eye irritant (ACGIH 1980).
Diethylaminoethanol(DEAE) is permitted by the U.S. Food and Drug Administration for some applications as a food additive. Applications include protective coatings for fresh fruits and vegetables, and as an additive in steam which directly contacts food products (excluding milk products). The National Research Council Committee on Toxicology (NRC 1983) has concluded that data on long-term, low-level airborne exposures of animals to DEAE for extrapolation to human health risks are severely lacking. This, combined with the lack of data concerning the concentrations of DEAE in humidified buildings did not allow sufficient information to set guidelines for long-term exposures or estimate the health risks from such exposures. The NRC was able to make some general recommendations based on the assumption that the nitrosation reactions (below) may occur, and that the amine should be considered as hazardous as the nitroso compound formed from it.

Carcinogenicity

DEAE was not mutagenic or clastogenic in a variety of in vitro and in vivo assays.
The 2003 ACGIH threshold limit valuetime- weighted average (TLV-TWA) for 2- diethylaminoethanol is 2 ppm (9.6mg/m3) with a notation for skin absorption.

Environmental Fate

DEAE, when compared with other amino alcohols, was observed to be biologically undecomposable in an experiment using activated sludge (HSDB 1988).

Metabolism

The absorption of DEAE (administered orally as DEAE acid malate or 'Cerebrol') in healthy adult rats is very rapid, reaching a peak plasma level in 30 min (Bismut et al 1986). The biological half-life is 3.5 h with 39% of the excreted product appearing in the urine after 48 h (Bismut et al 1986). In an earlier study, Schulte et al (1972) demonstrated that in rats, following a single oral dose, excretion occurs mainly through the kidneys with 37-59% being eliminated in the first 24 h. After 48 h, elimination was independent of dose. The brain and spinal cord showed the highest concentration after 7 d. Metabolites produced were observed to be diethylaminoethanol N-oxide, diethylaminoacetic acid, and ethylaminoethanol.

β-Diethylaminoethyl alcohol 2-DIETHYLAMINOETHANOL,REAGENT 1,2-DIETHYLAMINOETHANOL 2-DIETHYLAMINOETHANE Diethylethanolamin 2-(DIETHYLAMINO)-ETHANOL 99+% 2-diethylaminoethanol N,N-diethylethanolamine 2-DIETHYLAMINOETHANOL extrapure N,N-Diethylethanolamine, 99+% Ethanol, 2-(diethylamino)- 2-(Diethylamino)etha N,N-Diethylethanolamine (2-Hydroxyethyl)diethylamine N,N-Diethyletholamine N,N-DIETHYLETHANOLAMINE, A PRODUCT OF ATOFINA EUROPE 99,5+% 2-(DIETHYLAMINO)ETHANOL (N,N-DIETHYLETHA NOLAMIN) N,N-DIETHYLETHANOLAMINE, 99.5+% Rotec A.O. 2-DiethylaminoethanolForSynthesis Di-EthylEthanolamine(Deea) 2-ChloroethanolGr N-Diethylethanolamine 2-(Diethylamino)ethyl alcohol 2-(N,N-Diethylamino)ethanol 2-Hydroxytriethylamine beta-(Diethylamino)ethanol beta-(Diethylamino)ethyl alcohol beta-Hydroxytriethylamine Dehydasal Diaethylaminoaethanol Diethyl(2-hydroxyethyl)amine -Diethylamino Loramine AMB 13 N-(Diethylamino)ethanol N,N-Diethyl-2-hydroxyethylamine N,N-Diethylaminoethanol N,N-Diethylmonoethanolamine N,N-Diethyl-N-(beta-Hydroxyethyl)amine Pennad 150 Perdilaton DIETHYLAMINOETHANOL DIETHYLAMINOETHANOLAMINE DIETHYLAMLNOETHANOL DIETHYLETHANOLAMINE(N,N-) 2-(Diethylamino)ethanol >=99.5% (2-HYDROXYETHYL)DIETHYLAMINE 2-Diethylaminoehtanol 2 - Diethyl Amino Ethanol 100-37-8 1-(diethylamino)ethanol N,N-Diethylethanolamine (2-Diethylaminoethanol) Diethylaminoethanol USP/EP/BP 2-(Diethylamino)ethanol, puriss, 99%+ "N,N-Diethylethanol amine d4" 2-(Diethylamino)ethanol, puriss+ 2-Diethylaminoethanol (DEAE) extrapure, 99% DEEA DEAE N,N-Diethyl-2-aminoethanol DIETHYLETHANOLAMINE