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2-Hydroxyethylhydrazine

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CAS:109-84-2
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CAS:109-84-2
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2-Hydroxyethylhydrazine manufacturers

  • 2-Hydroxyethylhydrazine
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  • 2026-05-19
  • CAS:109-84-2
  • Min. Order: 1KG
  • Purity: 95%; 98%; 99%
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  • 2-Hydroxyethylhydrazine
  • 2-Hydroxyethylhydrazine pictures
  • $0.00 / 1KG
  • 2026-05-19
  • CAS:109-84-2
  • Min. Order: 1KG
  • Purity: 98%min
  • Supply Ability: 30tons/month
2-Hydroxyethylhydrazine Basic information
Product Name:2-Hydroxyethylhydrazine
Synonyms:1-(2-Hydroxyethyl)hydrazine;2-Hydrazineethanol;BETA-HYDROXYETHYL HYDRAZINE;ETHANOL-2-HYDRAZINE;HYDROXYETHYL HYDRAZINE;(2-Hydroxyethyl)drazine;2-Hydroxyethylhydrazine,97%;2-HYDROXYETHYLHYDRAZINE, TECH., 90%
CAS:109-84-2
MF:C2H8N2O
MW:76.1
EINECS:203-711-6
Product Categories:Pharmaceutical Intermediate;pharmacetical;Aliphatics
Mol File:109-84-2.mol
2-Hydroxyethylhydrazine Structure
2-Hydroxyethylhydrazine Chemical Properties
Melting point −70 °C(lit.)
Boiling point 155-160 °C32 mm Hg(lit.)
density 1.123 g/mL at 25 °C(lit.)
refractive index n20/D 1.493(lit.)
Fp 165 °F
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility soluble in DMSO, Methanol
pka14.79±0.10(Predicted)
form Liquid
color Colorless to Almost colorless
Water Solubility Soluble in water, alcohols and glycols.
Merck 13,4794
BRN 1731669
InChI1S/C2H8N2O/c3-4-1-2-5/h4-5H,1-3H2
InChIKeyGBHCABUWWQUMAJ-UHFFFAOYSA-N
SMILESNNCCO
CAS DataBase Reference109-84-2(CAS DataBase Reference)
NIST Chemistry Reference2-Hydroxyethylhydrazine(109-84-2)
EPA Substance Registry System2-Hydroxyethylhydrazine (109-84-2)
Safety Information
Hazard Codes T
Risk Statements 23/24/25-36/37/38-40-25
Safety Statements 23-26-36/37/39-45-60-20
RIDADR UN 2810 6.1/PG 3
WGK Germany 3
RTECS KL2800000
Hazard Note Toxic
TSCA TSCA listed
HazardClass 6.1
PackingGroup II
HS Code 29280000
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Carc. 2
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
2-Hydroxyethylhydrazine English
SigmaAldrich English
ALFA English
2-Hydroxyethylhydrazine Usage And Synthesis
Description 2-Hydroxyethylhydrazine (HEH) is the primary decomposition product of the high-energy ionic liquid 2-hydroxyethylhydrazinium nitrate (HEHN). As a hydrazine fuel, HEHN is the most widely used liquid monocomponent propellant in the aerospace sector. while HEH is a key target for investigating the reaction mechanism of HEHN.
Chemical PropertiesClear colorless oily liquid
Uses(2-Hydroxyethyl)hydrazine is used as a plant growth regulant, a component in jet fuels, intermediate for organic synthesis especially heterocycles used in agrochemicals, pharmaceuticals, stabilizers and polymerizations, Chain extender for urethane formulations, corrosion inhibitor.
Uses 2-Hydroxyethylhydrazine is used as an intermediate, plant growth regulator, flowering inducer for pineapples.
Preparation2-Hydroxyethylhydrazine is prepared by heating about 2 to 17 parts of hydrazine hydrate dissolved in water to about 30℃ to about 100℃. in a closed system. Then, 1 part of ethylene oxide is gradually added to the hydrazine hydrate, and the temperature of the reaction mixture is maintained in the range of about 30℃ to 70℃ during the addition.
DefinitionChEBI: 2-hydrazinoethanol is a member of hydrazines. It has a role as a herbicide. It is functionally related to an ethanol.
General Description2-Hydroxyethylhydrazine reacts with β-diketones having strong electron-withdrawing substituents to yield 5-hydroxy-4,5-dihydropyrazoles.
HazardModerate fire risk. Irritant.
Biological Activity2-Hydroxyethylhydrazine (HEH) is a potent and highly specific inhibitor of the phosphatidylethanolamine methylation pathway in Saccharomyces cerevisiae. Following HEH addition to culture medium, the incorporation of L-[3-14C]serine, L-[methyl-14C]methionine, and S-adenosyl-L-[methyl-14C]methionine into phosphatidylcholine was markedly reduced. In the presence of this inhibitor, cells ceased growth with an IC50 value of 66 pM. Although cellular activity remained unaffected, the addition of choline restored cell growth. This indicates that active phospholipid methylation is unnecessary as long as phosphatidylcholine is supplied via the CDP-choline pathway. The restoration of cell growth by choline suggests that HEH's primary target in vivo is phospholipid methylation.
Synthesis
ETHYLENE OXIDE

75-21-8

2-Hydroxyethylhydrazine

109-84-2

The general procedure for synthesizing 2-hydrazinoethanol from ethylene oxide was as follows: ethylene oxide was added to a VO1 liquefied gas storage tank and pressurized to 1.0~1.5 MPa using nitrogen. 80% hydrazine hydrate was added to a VO2 storage tank, and the molar ratio of hydrazine hydrate to ethylene oxide was controlled to be 8:1. the hydrazine hydrate was fed at a total feed flow rate of 2.0 L/h via feed pumps PO1 and PO2, respectively. The temperature of the micro-mixer was maintained at 40°C, the temperature of the cracking reactor was set at 60°C, the temperature of the micro-heat exchanger was controlled in the range of 0-10°C, and the back pressure of the back-pressure valve was set at 1.5-2.5 MPa. The two liquid feedstocks were mixed in a CPMM-R300 micro-mixer and then entered into the cracking reactor for further reaction. The reaction liquid is cooled by a micro heat exchanger and then micro-fed to the receiving vessel. Most of the water and excess hydrazine hydrate were removed by decompression distillation, and the final colorless oily liquid 2-hydroxyethylhydrazine was obtained. The purity of the product was 89.5% and the yield was 98% by GC. Finally, the entire microreactor system was washed using water.

References[1] Patent: CN104876833, 2016, B. Location in patent: Paragraph 0037; 0038
[2] Patent: EP2952509, 2015, A1. Location in patent: Paragraph 0041; 0042
[3] Bulletin de la Societe Chimique de France, 1939, vol. <5> 6, p. 708,714
[4] Ukrainskii Khimicheskii Zhurnal (Russian Edition), 1928, vol. 3, p. 125,128
[5] Chem. Zentralbl., 1930, vol. 101, # I, p. 2867
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