Product
Supplier
Encyclopedia
Inquiry
Home > Encyclopedia > 2-hydroxyethyl carbamate

2-hydroxyethyl carbamate

2-hydroxyethyl carbamate structure

2-hydroxyethyl carbamate 

structure
  • CAS No:

    5395-01-7

  • Formula:

    C3H7NO3

  • Chemical Name:

    2-hydroxyethyl carbamate

  • Synonyms:

    HYDROXYETHYLCARBAMATE;Carbamic acid 2-hydroxyethyl;Carbamic acid 2-hydroxyethyl ester;1,2-Ethanediol, 1-carbamate

2-hydroxyethyl carbamate Basic Attributes

105.09

105.09

MXE9F638CE

3139

TSCA listed

Crystalline solid|Clear, pale yellow, slightly viscous liquid ... may solidify at temperatures below 30 °C

Characteristics

log Kow = 1.48 /Estimated/

1.3895 (rough estimate)

43 °C

197.09°C (rough estimate)

370 °F

1.4368 (estimate)

Soluble in acetone and alcohol; insoluble in benzene and chloroform|Miscible with water

2.55 mm Hg at 25 °C /Estimated/

Ammoniacal

Henry's Law constant = 1.92X10-12 atm-cu m/mole at 25 °C /Estimated/

Deliquescent|Hydroxyl radical rate constant = 12.4X10-12 cu cm/molec-sec at 25 °C /Estimated/

Safety Information

SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.

|Warning|H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]|P264, P280, P305+P351+P338, and P337+P313|Aggregated GHS information provided by 96 companies from 3 notifications to the ECHA C&L Inventory.

Combustible.

Drug Information

When human liver microsomes were incubated with NADPH and ethyl carbamate, the products vinyl carbamate, 2-hydroxyethyl carbamate, and ethyl N-hydroxycarbamate were detected. When the reaction was done with ethyl carbamate as the substrate, the rate of product formation was nearly first order in ethyl carbamate concentration (Km greater than 2 mM) and the rate was considerably slower than in the case of vinyl carbamate. ... A large kinetic deuterium isotope effect (greater than 7) was observed for the formation of 1,N6-ethenoadenosine from ethyl carbamate, and high isotope effects (6-8) were also noted for the formation of vinyl carbamate and 2-hydroxyethyl carbamate.

In the present study, /hydroxyethyl carbamate/ HEC was synthesized by reacting ethylene carbonate with ammonia and was characterized. A single dose of HEC or /ethyl carbamate/ EC in saline was injected i.p. into adult male strain A mice, which were maintained for 16 weeks. HEC doses of 1.12, 4.6 and 11.2 mmol/kg induced 0.16, 0.32 and 0.32 lung adenomas/mouse, respectively. The 28% tumor incidence for the two highest doses was significantly (P < 0.05) greater than that in controls injected with saline alone. The number of tumors/mouse with 4.6 mmol HEC/kg was one-fortieth of that for an equimolar dose of EC. The weak activity of HEC supports the view that HEC is not a proximal carcinogenic metabolite of EC, i.e. that vinyl carbamate is produced directly from EC.|The carbamates alone weakly activated estrogen- or progesterone-responsive reporter genes in breast and endometrial cancer cells. All of the carbamates decreased estradiol- or progesterone-induced reporter gene activity in the breast and endometrial cancer cells. In whole cell competition binding assays, the carbamates demonstrated a limited capacity to displace radiolabeled estrogen or progesterone from /estrogen receptor/ or /progesterone receptor/. /Carbamates/

Basic treatment: Establish a patent airway. Suction if necessary. Watch for signs of respiratory insufficiency and assist ventilations if needed. Administer oxygen by nonrebreather mask at 10 to 15 L/min. Monitor for pulmonary edema and treat if necessary ... . Monitor for shock and treat if necessary ... . Anticipate seizures and treat if necessary ... . For eye contamination, flush eyes immediately with water. Irrigate each eye continuously with normal saline during transport ... . Do not use emetics. For ingestion, rinse mouth and administer 5 ml/kg up to 200 ml of water for dilution if the patient can swallow, has a strong gag reflex, and does not drool ... . Cover skin burns with dry sterile dressings after decontamination ... . /Poison A and B/|Advanced treatment: Consider orotracheal or nasotracheal intubation for airway control in the patient who is unconscious, has severe pulmonary edema, or is in respiratory arrest. Positive pressure ventilation techniques with a bag valve mask device may be beneficial. Monitor cardiac rhythm and treat arrhythmias as necessary ... . Start an IV with D5W /SRP: "To keep open", minimal flow rate/. Use lactated Ringer's if signs of hypovolemia are present. Watch for signs of fluid overload. Consider drug therapy for pulmonary edema ... . For hypotension with signs of hypovolemia, administer fluid cautiously. Watch for signs of fluid overload ... . Treat seizures with diazepam (Valium) ... . Use proparacaine hydrochloride to assist eye irrigation ... . /Poison A and B/

2-HEC

2-hydroxyethyl carbamate Use and Manufacturing

Uses

FORMERLY A CHEM INT FOR TEXTILE PERMANENT PRESS FINISHES|... a reactive intermediate in the manufacture of automotive coatings

Production

(1972) NEGLIGIBLE (EST)|(1975) No data

1,2-Ethanediol, 1-carbamate: ACTIVE|PMN - indicates a commenced PMN (Pre-Manufacture Notices) substance.|U.S patent 6,106951; U.S. patent 5,994,479

Scan the QR Code to Share

Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.