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Merck

774405

Sigma-Aldrich

(S)-2-氨基丁烷-1,4-二硫醇 盐酸盐

99% (titration)

别名:

(S)-2-氨基丁烷-1,4-二硫醇 盐酸盐, (2S)-2-氨基-1,4-二巯基丁烷 盐酸盐, DTBA, 二硫代丁胺

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About This Item

经验公式(希尔记法):
C4H11NS2 · HCl
分子量:
173.73
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.22

化驗

99% (titration)

形狀

solid

反應適用性

reagent type: reductant

mp

210-225 °C

儲存溫度

2-8°C

SMILES 字串

Cl.N[C@H](CS)CCS

InChI

1S/C4H11NS2.ClH/c5-4(3-7)1-2-6;/h4,6-7H,1-3,5H2;1H/t4-;/m0./s1

InChI 密鑰

HWWPXJZINVJNBM-WCCKRBBISA-N

應用

二硫代丁胺或DTBA是一种新型生物还原剂,其性能优于其他常用试剂。DTBA被证明比DTT还原小分子二硫化物快3-5倍,并且与DTT相比,还原(激活)半胱氨酸依赖性蛋白酶木瓜蛋白酶的速度快14倍。另外,由于伯胺基的存在,使得从混合物中去除DTBA的过程变得更加简单,并且可以使用阳离子交换树脂来实现。
S)-2-氨基丁烷-1,4-二硫醇盐酸盐(DTBA),也称为二硫代丁胺,是一种生物还原剂,具有比其他常用试剂更高的性能。 DTBA被证明比DTT还原小分子二硫化物快3-5倍,并且与DTT相比,还原(激活)半胱氨酸依赖性蛋白酶木瓜蛋白酶的速度快14倍。 另外,由于伯胺基的存在,使用后从混合物中去除DTBA的过程得到简化,并且可以使用阳离子交换树脂来实现。

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Javier Troyano et al.
Inorganic chemistry, 58(5), 3290-3301 (2019-02-13)
Direct reactions under ambient conditions between CuX (X = Br, I) and thiobenzamide (TBA) were carried out at different ratios, giving rise to the formation of a series of one-dimensional (1D) coordination polymers, (CPs) [CuI(TBA)] n (1), [Cu3I3(TBA)2] n (4)
Coordination properties of dithiobutylamine (DTBA), a newly introduced protein disulfide reducing agent.
Adamczyk J, et al.
Inorganic Chemistry, 54(2), 596-606 (2014)
A potent, versatile disulfide-reducing agent from aspartic acid.
Lukesh III, et al.
Journal of the American Chemical Society, 134(9), 4057-4059 (2012)
Mozhdeh Imaninezhad et al.
Bioconjugate chemistry, 30(1), 34-46 (2018-12-19)
Macroporous cell-laden hydrogels have recently gained recognition for a wide range of biomedical and bioengineering applications. There are various approaches to create porosity in hydrogels, including lyophilization or foam formation. However, many do not allow a precise control over pore
Sean B Johnston et al.
PloS one, 10(1), e0116898-e0116898 (2015-01-22)
Phosphatase and tensin homologue deleted from chromosome ten (PTEN) is a lipid phosphatase tumor suppressor that is lost or inactivated in most human tumors. The enzyme catalyzes the hydrolysis of phosphatidylinositol-(3,4,5)-trisphosphate (PIP3) to form phosphatidylinositol-(4,5)-bisphosphate (PIP2) and inorganic phosphate. Here

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Professor Ron Raines works with Sigma-Aldrich on the development of reagents and tools for chemical biology such as the traceless Staudinger ligation reagent (670359). DTBA (774405), a superior biological reducing reagent to DTT, is another technology to come out of the Raines lab.

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