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Merck
CN

88640

1-硫代甘油

≥99.0% (GC)

别名:

α-单硫代甘油, α-硫代甘油, 3-巯基-1,2-丙二醇

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关于此项目

线性分子式:
HSCH2CH(OH)CH2OH
化学文摘社编号:
分子量:
108.16
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
EC Number:
202-495-0
Beilstein/REAXYS Number:
1732046
MDL number:
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Quality Level

assay

≥99.0% (GC)

form

liquid

refractive index

n20/D 1.527 (lit.), n20/D 1.528

bp

118 °C/5 mmHg (lit.)

density

1.25 g/mL at 25 °C (lit.)

SMILES string

OCC(O)CS

InChI

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

InChI key

PJUIMOJAAPLTRJ-UHFFFAOYSA-N

Application

1-硫代甘油,一种衍生化试剂,被用于研究含水硫醇封端CdTe纳米晶体的pH敏感性光致发光。1-硫代甘油被用于开发和测试硫醇官能化共聚物。1-硫代甘油被用作后修饰剂,用于非标准肽折叠体的生成。
2-巯基乙醇的潜在替代物;作为淋巴细胞活化研究的探针

Preparation Note

本品可与乙醇(1 ml/ml,50%,v/v)混溶,得到澄清无色溶液。 它也可以与水混溶(0.1 M)。


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pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

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

存储类别

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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M G Goodman et al.
The Journal of experimental medicine, 145(3), 473-489 (1977-03-01)
The effect of 2-mercaptoethanol (2-ME) and alpha-thioglycerol (alpha TG) on proliferation and polyclonal activation of lymphocytes was studied in cultures of spleen cells from C3H mice. Inclusion in serum-free or serum-containing medium of the optimal concentration (5 x 10(-5) M)
Kimiko Ishiguro et al.
Molecular cancer therapeutics, 4(11), 1755-1763 (2005-11-09)
Cloretazine (VNP40101M; 101M; 1,2-bis(methylsulfonyl)-1-(2-chloroethyl)-2-[(methylamino)carbonyl]hydrazine) is a sulfonylhydrazine prodrug that generates both chloroethylating and carbamoylating species on activation. To explore the molecular mechanisms underlying the broad anticancer activity observed in preclinical studies, cloretazine and chloroethylating-only [i.e., 1,2-bis(methylsulfonyl)-1-(2-chloroethyl)hydrazine] and carbamoylating-only (i.e., 1,2-bis(methylsulfonyl)-1-[(methylamino)carbonyl]hydrazine)
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



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货号GTIN
88640-100ML04061833065129
88640-500ML04061833065136