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HomeProduct name list2-Mercaptoethanol

2-Mercaptoethanol

Synonym(s):β-Mercaptoethanol;2-Hydroxyethylmercaptan;2-Mercaptoethanol;BME;Thioethylene glycol

  • CAS NO.:60-24-2
  • Empirical Formula: C2H6OS
  • Molecular Weight: 78.13
  • MDL number: MFCD00004890
  • EINECS: 200-464-6
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-12-18 14:15:32
2-Mercaptoethanol Structural

What is 2-Mercaptoethanol?

Chemical properties

2-mercaptoethanol(bME) is a clear colorless liquid. It is a popular effective reducer, but extremely pungent.

The Uses of 2-Mercaptoethanol

2-Mercaptoethanol is used in the preparation of nano-graphene for cellular imaging and drug delivery as well as multifunctional polymeric micelle. It acts as a reducing agent used in electrophoresis, amino acid detection, and distinguishing ssDNA/dsDNA. It is also employed as a standard buffer. It is also used in the preparation of PVC heat stabilizers and as a chain transfer agent in the manufacture of PVC. Further, it is used in some RNA isolation procedures to eliminate ribonuclease. It is utilized as a corrosion inhibitor and ore floatation agent. In biochemistry, it is useful to study the activity of the immune system. Solubilizes proteins by reducing disulfide linkages.

What are the applications of Application

β-Mercaptoethanol is a reducing agent used in electrophoresis, amino acid detection, and distinguishing ssDNA/dsDNA)

Definition

ChEBI: 2-Mercaptoethanol is a primary alcohol and an alkanethiol. It has a role as a geroprotector.

What are the applications of Application

2-Mercaptoethanol is used in the synthesis of nano-graphene for cellular imaging and drug delivery. Also used in the synthesis of multifunctional polymeric micelle used in specific targeting of tumor disruption.

General Description

A water-white liquid. May be toxic by ingestion, inhalation, or skin absorption.

Air & Water Reactions

No rapid reaction with air. No rapid reaction with water.

Reactivity Profile

Organosulfides, such as 2-Mercaptoethanol, are incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials generate heat and in many cases hydrogen gas. Many of these compounds may liberate hydrogen sulfide upon decomposition or reaction with an acid.

Hazard

Toxic by inhalation and ingestion.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Safety Profile

Poison by ingestion, skin contact, and intraperitoneal routes. Moderately toxic by intravenous route. A skin and severe eye irritant. Human mutation data reported. A combustible liquid when exposed to heat, flame, or oxidizers. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits highly toxic fumes of SOx. See also MERCAPTANS.

Purification Methods

Purify it by distilling in a vacuum. Distilling at atmospheric pressure causes some oxidation and should be done in an inert atmosphere. [Woodward J Chem Soc 1892 1948.] It has a foul odour, is irritating t o the eyes, nose and skin — should be handled in an efficient fume cupboard. It is miscible with H2O, EtOH, Et2O and *C6H6 and the UV has max at 235nm. The 2,4-dinitrophenyl thioether has m 101-102o (from EtOH or aqueous MeOH) [Grogen et al. J Org Chem 20 50 1955]. [Beilstein 1 IV 2428.]

Properties of 2-Mercaptoethanol

Melting point: -100 °C
Boiling point: 157 °C (lit.)
Density  1.114 g/mL at 25 °C (lit.)
vapor density  2.69 (vs air)
vapor pressure  1 mm Hg ( 20 °C)
refractive index  n20/D 1.500(lit.)
FEMA  4582 | 2-HYDROXYETHANETHIOL
Flash point: 165 °F
storage temp.  Store below +30°C.
solubility  H2O: 1 mL/mL
form  liquid
pka 9.72(at 25℃)
Specific Gravity 1.119 (20/4℃)
color  Clear colorless to slightly yellow
Odor Disagreeable odor
PH 4.5-6 (500g/l, H2O, 20℃)
PH Range 4.5 - 6 at 500 g/l at 20 °C
explosive limit 2.3-18%(V)
Water Solubility  soluble
FreezingPoint  <100℃
Sensitive  Air Sensitive & Hygroscopic
λmax λ: 260 nm Amax: 1.5
λ: 280 nm Amax: 0.3
JECFA Number 1925
Merck  14,5869
BRN  773648
Stability: Air Sensitive
CAS DataBase Reference 60-24-2(CAS DataBase Reference)
NIST Chemistry Reference Ethanol, 2-mercapto-(60-24-2)
EPA Substance Registry System 2-Mercaptoethanol (60-24-2)

Safety information for 2-Mercaptoethanol

Signal word Danger
Pictogram(s)
ghs
Corrosion
Corrosives
GHS05
ghs
Skull and Crossbones
Acute Toxicity
GHS06
ghs
Health Hazard
GHS08
ghs
Environment
GHS09
GHS Hazard Statements H310:Acute toxicity,dermal
H315:Skin corrosion/irritation
H317:Sensitisation, Skin
H318:Serious eye damage/eye irritation
H373:Specific target organ toxicity, repeated exposure
H410:Hazardous to the aquatic environment, long-term hazard
Precautionary Statement Codes P273:Avoid release to the environment.
P280:Wear protective gloves/protective clothing/eye protection/face protection.
P301+P310:IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Computed Descriptors for 2-Mercaptoethanol

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