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この商品について
化学式:
HSCH2CH2OH
CAS番号:
分子量:
78.13
UNSPSC Code:
23151817
NACRES:
NA.05
PubChem Substance ID:
EC Number:
200-464-6
Beilstein/REAXYS Number:
773648
MDL number:
製品名
2-メルカプトエタノール, derivatization grade (HPLC), LiChropur™, ≥99.0% (GC)
InChI
1S/C2H6OS/c3-1-2-4/h3-4H,1-2H2
InChI key
DGVVWUTYPXICAM-UHFFFAOYSA-N
SMILES string
OCCS
grade
derivatization grade (HPLC)
vapor density
2.69 (vs air)
vapor pressure
1 mmHg ( 20 °C)
assay
≥99.0% (GC)
form
liquid
quality
LiChropur™
expl. lim.
18 %
concentration
14.3 M (pure liquid)
technique(s)
HPLC: suitable
refractive index
n20/D 1.500 (lit.)
n20/D 1.500-1.502
bp
157 °C (lit.)
density
1.114 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
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関連するカテゴリー
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.
suitable for derivatisation of Amine groups
General description
2-Mercaptoethanol is a thiol compound showing growth promoting properties on mouse lymphoma L1210 cells in vitro. It also enhances viability, blast transformation and antibody formation in lymphocyte cultures.
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
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. 1A - STOT RE 2 Oral
target_organs
Liver,Heart
保管分類
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
165.2 °F - closed cup
flash_point_c
74 °C - closed cup
Mechanism of growth stimulation of L1210 cells by 2-mercaptoethanol in vitro. Role of the mixed disulfide of 2-mercaptoethanol and cysteine
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