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102185-33-1 分子结构
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disodium 5-bromo-4-chloro-1H-indol-3-yl phosphate

ChemBase编号:102949
分子式:C8H4BrClNNa2O4P
平均质量:370.431961
单一同位素质量:368.85452249
SMILES和InChIs

SMILES:
[Na+].[Na+].[O-]P(=O)([O-])Oc1c[nH]c2c1c(Cl)c(Br)cc2
Canonical SMILES:
Clc1c(Br)ccc2c1c(c[nH]2)OP(=O)([O-])[O-].[Na+].[Na+]
InChI:
InChI=1S/C8H6BrClNO4P.2Na/c9-4-1-2-5-7(8(4)10)6(3-11-5)15-16(12,13)14;;/h1-3,11H,(H2,12,13,14);;/q;2*+1/p-2
InChIKey:
OAZUOCJOEUNDEK-UHFFFAOYSA-L

引用这个纪录

CBID:102949 http://www.chembase.cn/molecule-102949.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
disodium 5-bromo-4-chloro-1H-indol-3-yl phosphate
IUPAC传统名
dipotassium 5-bromo-4-chloro-1H-indol-3-yl phosphate
disodium 5-bromo-4-chloro-1H-indol-3-yl phosphate
别名
5-溴-4-氯-3-吲哚磷酸 二钠盐
BCIP
X-phosphate
5-BROMO-4-CHLORO-3-INDOLYL PHOSPHATE DISODIUM SALT
BCIP®
X-phosphate disodium salt
5-Bromo-4-chloro-3-indolyl phosphate disodium salt
CAS号
102185-33-1
MDL号
MFCD00036757
PubChem SID
162089603
PubChem CID
6097197

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
PubChem 6097197 external link

理论计算性质

理论计算性质

JChem
Acid pKa 1.726015  质子受体
质子供体 LogD (pH = 5.5) 0.10124553 
LogD (pH = 7.4) -0.6621499  Log P 2.4873745 
摩尔折射率 60.1825 cm3 极化性 25.167912 Å3
极化表面积 88.21 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

理化性质 安全信息 产品相关信息 生物活性(PubChem)
溶解度
DMF: insoluble expand 查看数据来源
H2O: soluble20 mg/mL expand 查看数据来源
外观
powder expand 查看数据来源
熔点
> 300°C expand 查看数据来源
保存条件
0°C, Desiccate, Protect from light expand 查看数据来源
-20°C, Desiccate, Protect from light expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
3 expand 查看数据来源
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand 查看数据来源
保存温度
-20°C expand 查看数据来源
纯度
>98% expand 查看数据来源
≥98% expand 查看数据来源
≥98.0% (HPLC) expand 查看数据来源
99% expand 查看数据来源
级别
for molecular biology expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
Foreign Activity
Protease, none detected expand 查看数据来源
线性分子式
C8H4BrClNO4P · 2Na expand 查看数据来源

详细说明

详细说明

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich
MP Biomedicals -  02150042 external link
Substrate for alkaline phosphatase
Purity: 99%
MP Biomedicals -  02193989 external link
Molecular Biology Reagent
Disodium Salt
Purity: >98%
Chromogenic substrate for alkaline phosphatase in ELISA.
Sigma Aldrich -  B1026 external link
Substrates
Histochemical substrate for alkaline phosphatase.
Application
For the colorimetric detection of alkaline phosphatase-labeled molecules, 5-Bromo-4-chloro-3-indolyl phosphate (BCIP) and Nitro Blue Tetrazolium (NBT) are available. The BCIP/NBT substrate system is versatile and functions in a variety of applications, including Northern Southern, and Western blotting, in situ hybridization, and immunohistochemistry. BCIP is provided in two salt forms: the disodium salt which is soluble in water and the p-toluidine form which is soluble in dimethylformamide. These salt forms may be used to prepare a stock solution that in combination with NBT and a reaction buffer, form a substrate solution for alkaline phosphatase. This substrate system, when incubated with alkaline phosphatase, produces an insoluble NBT diformazan product that is easily observable with its purple color. For added convenience, a mixture of BCIP and NBT is provided in an easily dissolvable tablet form or as a ready-to-use liquid.
法律信息
BCIP 注册商标 Sigma-Aldrich Co. LLC
Sigma Aldrich -  16668 external link
Other Notes
For visualizing antigenic proteins immobilized on nitrocellulose paper1,2
Substrates
Histochemical substrate for alkaline phosphatase.
Application
For the colorimetric detection of alkaline phosphatase-labeled molecules, 5-Bromo-4-chloro-3-indolyl phosphate (BCIP) and Nitro Blue Tetrazolium (NBT) are available. The BCIP/NBT substrate system is versatile and functions in a variety of applications, including Northern Southern, and Western blotting, in situ hybridization, and immunohistochemistry. BCIP is provided in two salt forms: the disodium salt which is soluble in water and the p-toluidine form which is soluble in dimethylformamide. These salt forms may be used to prepare a stock solution that in combination with NBT and a reaction buffer, form a substrate solution for alkaline phosphatase. This substrate system, when incubated with alkaline phosphatase, produces an insoluble NBT diformazan product that is easily observable with its purple color. For added convenience, a mixture of BCIP and NBT is provided in an easily dissolvable tablet form or as a ready-to-use liquid.
法律信息
BCIP 注册商标 Sigma-Aldrich Co. LLC

参考文献

参考文献

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专利

专利

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