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M1753

Sigma-Aldrich

1-tioglicerol

≥97%

Sinônimo(s):

αα-monotioglicerol, α1-tioglicerol, 3-Mercapto-1,2-propanodiol

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About This Item

Fórmula linear:
HSCH2CH(OH)CH2OH
Número CAS:
96-27-5
Peso molecular:
108.16
Beilstein:
1732046
Número CE:
202-495-0
Número MDL:
MFCD00004879
Código UNSPSC:
12352201
ID de substância PubChem:
24896684
NACRES:
NA.25

Ensaio

≥97%

Formulário

liquid

índice de refração

n20/D 1.527 (lit.)

p.e.

118 °C/5 mmHg (lit.)

densidade

1.25 g/mL at 25 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

OCC(O)CS

InChI

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

chave InChI

PJUIMOJAAPLTRJ-UHFFFAOYSA-N

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Descrição geral

1-Thioglycerol stimulates the synthesis of porphyrin in aerobically growing Escherichia coli. It is an inhibitor of glycerol kinase activity in vitro and in situ.

Aplicação

1-Thioglycerol has been used in a study to assess the manipulation of aqueous growth of CdTe nanocrystals. It has also been used in a study that investigated the effect of surface attachment on ligand binding.

Nota de preparo

This product is miscible in ethanol (1 ml/ml, 50%, v/v), yielding a clear, colorless solution. It is also miscible in water (0.1 M).

Pictogramas

Skull and crossbones
GHS06

Palavra indicadora

Danger

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

210.2 °F - closed cup

Ponto de fulgor (°C)

99 °C - closed cup

Equipamento de proteção individual

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

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Certificados de análise (COA)

Lot/Batch Number
MKCQ6881
MKCQ7140
MKCQ6880
MKCQ6878
MKCQ6879

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Sigma-Aldrich

328375

1-Mercapto-2-propanol

Bathocuproinedisulfonic acid disodium salt for spectrophotometric det. of Cu, Fe

Sigma-Aldrich

B1125

Bathocuproinedisulfonic acid disodium salt

D-(−)-Frutose ≥99% (HPLC)

Sigma-Aldrich

F0127

D-(−)-Frutose

Hao Zhang et al.
Journal of the American Chemical Society, 128(31), 10171-10180 (2006-08-03)
The present article is devoted to systematically exploring the influence of various experimental variables, including the precursor concentration, the ligand nature, the counterion type, the Cd-to-Te molar ratio, pH, and temperature, on the aqueous growth of CdTe nanocrystals. The growth
G T Javor et al.
Journal of bacteriology, 174(3), 1072-1075 (1992-02-01)
1-Thioglycerol (TG) stimulates the synthesis of porphyrin in aerobically growing Escherichia coli. Here the levels of delta-aminolevulinate biosynthetic enzymes in untreated and TG-treated E. coli THU and PUC2 (a mutant of THU which overproduces porphyrins in the presence of thiols)
P Tengvall et al.
Biomaterials, 17(10), 1001-1007 (1996-05-01)
Thiol-modified surfaces are chemically well defined and suited for surface biological model experiments and biomaterials research. 3-Mercapto-1,2-propanediol (mercaptoglycerol, MG), immobilized on gold, spontaneously binds immunoglobulins from human serum and activates the complement system. The surface-bound complement factors were detected by
Jonas Wetterö et al.
Biomaterials, 23(4), 981-991 (2002-01-17)
Since the realization of a complement activation capacity by artificial surfaces upon contact with blood, a common belief has evolved that charged nucleophilic surface groups such as amine (-NH2) and hydroxyl (-OH) react with and eventually bind to the internal
Valérie Gagnard et al.
Bioorganic & medicinal chemistry, 12(6), 1393-1402 (2004-03-17)
A new enzyme-labile group called S-acyl-3-thiopropyl group (SATP) has been synthesized from allylic esters of phosphonate. After demonstration of the enzyme-labile character of the SATP in cellular extracts, it has been introduced onto the phosphonate moiety of PFA (Foscarnet) to
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