所有图片(2)
About This Item
经验公式（希尔记法）:
C10H11BrN2O2
CAS号:
分子量:
271.11
Beilstein:
4430959
MDL號碼:
分類程式碼代碼:
12171500
PubChem物質ID:
NACRES:
NA.47
推荐产品
![MBCL [单氯二胺] suitable for fluorescence, ≥70.0% (HPCE)](/deepweb/assets/sigmaaldrich/product/structures/260/542/d42965bb-446e-4861-90c2-db4172b96abc/640/d42965bb-446e-4861-90c2-db4172b96abc.png)
product name
溴乙烷, ≥97% (HPLC)
品質等級
化驗
≥97% (HPLC)
形狀
powder
顏色
yellow
mp
161 °C
溶解度
acetonitrile: 20 mg/mL
&epsilon ；(消光係數)
4.6-5.1 at 396-398 nm in H2O
應用
diagnostic assay manufacturing
hematology
histology
儲存溫度
−20°C
SMILES 字串
CC1=C(C)C(=O)N2N1C(CBr)=C(C)C2=O
InChI
1S/C10H11BrN2O2/c1-5-7(3)12-8(4-11)6(2)10(15)13(12)9(5)14/h4H2,1-3H3
InChI 密鑰
AHEWZZJEDQVLOP-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
一般說明
溴代双满又称单溴联苯胺。它还是一种已知的硫醇探针，是一种在光解反应后活化的荧光试剂。
應用
溴代双满用于高效液相色谱法硫醇测定,适于荧光测定2，3-二巯基丙烷-1-磺酸和其他二硫醇。溴代双满已用作研究牛心线粒体寡霉素敏感性 ATP 酶的荧光标记。
此物质可用于体内和体外游离硫化氢的定量测定。它已用于标记含有硫醇基的蛋白质。
此物质可用于体内和体外游离硫化氢的定量测定。它已用于标记含有硫醇基的蛋白质。
生化／生理作用
溶液形式的溴代双满可与小分子硫醇基（如 GSH）和反应性蛋白硫醇基（如血红蛋白）反应。溴代双满与硫醇的反应为二级pH依赖性反应，且在与硫醇盐反应后，可活化水溶性荧光产物以便检测。
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
個人防護裝備
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
分析证书(COA)
Lot/Batch Number
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
其他客户在看
Differing effects of mechanical dough development and sheeting development methods on aggregated glutenin proteins.
Sutton KH, et al.
Cereal Chem., 80.6, 707-711 (2003)
Brigitte Bauer et al.
Chemical research in toxicology, 24(5), 737-743 (2011-04-14)
Allergic contact dermatitis is the most prevalent form of human immunotoxicity. It is caused by reactive low molecular weight chemicals, that is, haptens, coming in contact with the skin where hapten-peptide complexes are formed, activating the immune system. By using
N S Kosower et al.
Proceedings of the National Academy of Sciences of the United States of America, 76(7), 3382-3386 (1979-07-01)
The bimane fluorescent labels, monobromobimane, dibromobimane, and monobromotrimethylammoniobimane, are derivatives of syn-9,10-dioxabimane:1,5-diazabicyclo[3.3.0]octa-3,6-diene-2,8-dione. They efficiently label hemoglobin (reactive thiol groups), membrane proteins, and glutathione of normal human red cells under physiological conditions. Monobromobimane and dibromobimane are effective on intact cells while
Michael Hall et al.
Proteomics, 10(5), 987-1001 (2010-01-06)
The light-dependent regulation of stromal enzymes by thioredoxin (Trx)-catalysed disulphide/dithiol exchange is known as a classical mechanism for control of chloroplast metabolism. Recent proteome studies show that Trx targets are present not only in the stroma but in all chloroplast
Florencia Sardi et al.
Analytical biochemistry, 435(1), 74-82 (2013-01-09)
A method based on the differential reactivity of thiol and thiolate with monobromobimane (mBBr) has been developed to measure nucleophilicity and acidity of protein and low-molecular-weight thiols. Nucleophilicity of the thiolate is measured as the pH-independent second-order rate constant of
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门