137151

2-Mercaptoethanol

EMPROVE® EVOLVE

Manufacturer: SAFC

CAS Number: 60-24-2

Synonym(S): β-Mercaptoethanol, 2-Hydroxyethylmercaptan, BME, Thioethylene glycol

Select a Size

Pack Size SKU Availability Price
100 ML 137151-100-ML In Stock ₹ 84,803.05

137151 - 100 ML

₹ 84,803.05

In Stock

Quantity

1

Base Price: ₹ 84,803.05

GST (18%): ₹ 15,264.549

Total Price: ₹ 1,00,067.599

vapor density

2.69 (vs air)

Quality Level

400

vapor pressure

1 mmHg ( 20 °C)

form

liquid

expl. lim.

18 %

concentration

14.3 M (pure liquid)99.0-101.0 % (w/w)

impurities

≤1.0% related substances (GC) 2,2-Dithiodiethanol

refractive index

n20/D 1.500 (lit.)

bp

157 °C (lit.)

density

1.114 g/mL at 25 °C (lit.)

Description

  • General description: Our SAFC® portfolio of high-quality raw materials for use in biopharmaceutical processing withstands strict quality control procedures plus the documentation and expertise to help our customers meet requirements as defined by the M-Clarity Program.M-Clarity ProgramAs part of our EMPROVE® Program, our raw materials are offered with EMPROVE® Dossiers which provide comprehensive, up-to-date documentation to help you navigate regulatory challenges, manage risks, and improve your manufacturing processes.Our comprehensive portfolio of upstream process chemicals not only provides biopharmaceutical manufacturers with high-quality raw materials for production of classical and novel therapies, but also helps them get to market faster and simplify regulatory challenges. Trust us to deliver supply chain transparency and reliable sourcing around the globe, streamlining your product qualification with best-in-class regulatory support and service.
  • Application: BME is suitable for reducing protein disulfide bonds prior to polyacrylamide gel electrophoresis and is usually included in a sample buffer for SDS-PAGE at a concentration of 5%. Cleaving intermolecular (between subunits) disulfide bonds allows the subunits of a protein to separate independently on SDS-PAGE. Cleaving intramolecular (within subunit) disulfide bonds allows the subunits to become completely denatured so that each peptide migrates according to its chain length with no influence due to secondary structure.
  • Analysis Note: purity (GC) ≥99.0%
  • Legal Information: Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany

SAFETY INFORMATION

Pictograms

GHS05,GHS06,GHS08,GHS09

Signal Word

Danger

Hazard Statements

H301 + H331 - H310 - H315 - H317 - H318 - H361fd - H373 - H410

Precautionary Statements

P201 - P260 - P280 - P301 + P310 + P330 - P302 + P352 + P310 - P305 + P351 + P338 + P310

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral

Storage Class Code

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(C)

74 °C - closed cup