Bromoacetic acid N-hydroxysuccinimide ester

• 产品号: B8271
• CAS号: 42014-51-7
• 分子式: C6H6BrNO4
• 分子量: 236.02014
• 纯 度: ~95%

产品别名

• 标题: Bromoacetic acid N-hydroxysuccinimide ester
• IUPAC标准名: 2,5-dioxopyrrolidin-1-yl 2-bromoacetate
• IUPAC传统名: 2,5-dioxopyrrolidin-1-yl 2-bromoacetate

产品登记号

• MDL号: MFCD00058571
• CAS号: 42014-51-7
• PubChem SID: 24892067

产品性质

• Empirical Formula (Hill Notation): C6H6BrNO4
• 纯度: ~95%
• 产品质量级别: PREMIUM
• 运输包装: dry ice
• 外观: powder
• 溶解度: acetone: soluble25 mg/mL
• 溶解度: DMF: soluble
• GHS警示词: Warning
• GHS危险声明: H315-H319-H335
• 欧盟危险性物质标志: 刺激性(Irritant) (Xi)
• 个人保护装置: dust mask type N95 (US), Eyeshields, Gloves
• GHS警示性声明: P261-P305 + P351 + P338
• 危险公开号: 36/37/38
• 安全公开号: 26-36
• 保存温度: -20°C
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Application
A heterobifunctional cross-linking reagent which allows bromoacetylation of primary amine groups followed by coupling to sulfhydryl-containing compounds. Typically, initial reaction couples via ester to primary amine by amide bond formation in the pH range 6.5-8.5. The second reaction results in thioether bonding in pH range 7.0-8.0.
Caution
The bromoacetyl group is light sensitive.

详细说明 (简体中文)

Application
A heterobifunctional cross-linking reagent which allows bromoacetylation of primary amine groups followed by coupling to sulfhydryl-containing compounds. Typically, initial reaction couples via ester to primary amine by amide bond formation in the pH range 6.5-8.5. The second reaction results in thioether bonding in pH range 7.0-8.0.
Caution
The bromoacetyl group is light sensitive.