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Merck

M6145

1-Thioglycerol

liquid, BioReagent, suitable for cell culture, ≥97% (titration)

Synonym(s):

α-Monothioglycerol, α-Thioglycerol, 3-Mercapto-1,2-propanediol

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About This Item

Linear Formula:
HSCH2CH(OH)CH2OH
CAS Number:
96-27-5
Molecular Weight:
108.16
UNSPSC Code:
12352211
NACRES:
NA.75
PubChem Substance ID:
24897080
EC Number:
202-495-0
Beilstein/REAXYS Number:
1732046
MDL number:
MFCD00004879

Key Documents

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InChI key

PJUIMOJAAPLTRJ-UHFFFAOYSA-N

InChI

1S/C3H8O2S/c4-1-3(5)2-6/h3-6H,1-2H2

SMILES string

OCC(O)CS

biological source

synthetic (organic)

product line

BioReagent

assay

≥97% (titration)

form

liquid

technique(s)

cell culture | mammalian: suitable, single cell analysis: suitable

Quality Level

200

refractive index

n20/D 1.527 (lit.)

bp

118 °C/5 mmHg (lit.)

solubility

water: miscible 0.1 M

density

1.25 g/mL at 25 °C (lit.)

storage temp.

2-8°C

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Application

Cell culture studies of embryonic cortical and hippocampal neurons, mouse bone marrow mast cell lines, and human Β cell lines have utilized 1-thioglycerol as a component of the culture medium to stimulate proliferation.

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Skin Irrit. 2 - Skin Sens. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

210.2 °F - closed cup

flash_point_c

99 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX8220
MKCW7593
MKCT6083
MKCV1220
MKCR2024

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Suji Lee et al.
Stem cells (Dayton, Ohio), 36(10), 1552-1566 (2018-07-14)
Although autologous induced pluripotent stem cells (iPSCs) can potentially be useful for treating patients without immune rejection, in reality it will be extremely expensive and labor-intensive to make iPSCs to realize personalized medicine. An alternative approach is to make use
Nadja Franz et al.
Organic & biomolecular chemistry, 7(24), 5207-5218 (2009-12-22)
Hydrophilic/hydrophobic patterning is a powerful strategy to control folding in non-natural polymers/oligomers. In this contribution, we present a novel strategy for the preparation of alternating hydrophilic/hydrophobic patterned non-natural peptide foldamers. This strategy relies on the post-modification of a reactive peptide
Doron Burshtain et al.
Physical chemistry chemical physics : PCCP, 8(1), 158-164 (2006-02-17)
The difference in the heterogeneous binding of Mg(2+), Ca(2+) and Sr(2+) ions by 1-thioglycerol (TG) and 1,4-dithiothreitol (DTT) spontaneously adsorbed monolayers on Au has been studied following the changes in the double layer capacity. A mathematical treatment, based on calculating
L Tang et al.
Journal of biomedical materials research, 41(2), 333-340 (1998-06-25)
Biomaterial-mediated complement activation repeatedly has been invoked as a trigger of phagocyte reactions and inflammation. However, a direct correlation between complement activation and inflammatory responses to biomaterial surfaces has yet to be established. Using an animal implantation model and gold
Morgan Oatley et al.
Nature communications, 11(1), 586-586 (2020-01-31)
The endothelial to haematopoietic transition (EHT) is the process whereby haemogenic endothelium differentiates into haematopoietic stem and progenitor cells (HSPCs). The intermediary steps of this process are unclear, in particular the identity of endothelial cells that give rise to HSPCs
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Product Information Sheet - M6145

Product Information Sheet

Global Trade Item Number

SKUGTIN
M6145-25ML04061834060680

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