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6-Aminofluorescein_分子结构_CAS_51649-83-3)
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6-Aminofluorescein

产品号 201634 公司名称 Sigma Aldrich
CAS号 51649-83-3 公司网站 http://www.sigmaaldrich.com
分子式 C20H13NO5 电 话 1-800-521-8956
分子量 347.32092 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 107077

产品价格信息

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产品别名

标题
6-Aminofluorescein
IUPAC标准名
6-amino-3',6'-dihydroxy-3H-spiro[2-benzofuran-1,9'-xanthene]-3-one
IUPAC传统名
6-amino-3',6'-dihydroxyspiro[2-benzofuran-1,9'-xanthene]-3-one
别名
Fluoresceinamine isomer II

产品登记号

MDL号 MFCD00005051
EC号 257-334-7
Beilstein号 51708
CAS号 51649-83-3
PubChem SID 24852016

产品性质

Empirical Formula (Hill Notation) C20H13NO5
紫外吸收波长 λmax 495 nm
熔点 285 °C (dec.)(lit.)
GHS危险品标识 GHS07
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) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
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
德国WGK号 3

产品详细信息

详细说明 (English)
Other Notes
Note: Do not confuse with fluorescamine.
Packaging
1, 5 g in glass bottle
250 mg in glass bottle
Application
6-Aminofluorescein has been demonstrated to be useful fluorescent labeling reagent for fullerene-based liposome nanostructures termed ‘buckysomes’1. 6-aminofluorescein dissolved in 0.1 N NaOH can be quantified from a maximum absorbance at 490 nm. Decarboxylated 6-aminofluorescein dissolved 6 N HCl (prepare by constant boiling at 110° C for 24 h) can be quantified from a maximum absorbance at 454 nm. Aldehyde groups are formed by oxidateive damage to proteins, which can be detected by conjugation to decarboxylated 6-aminofluorescein2.
详细说明 (简体中文)
Other Notes
Note: Do not confuse with fluorescamine.
包装
1, 5 g in glass bottle
250 mg in glass bottle
Application
6-Aminofluorescein has been demonstrated to be useful fluorescent labeling reagent for fullerene-based liposome nanostructures termed ‘buckysomes’1. 6-aminofluorescein dissolved in 0.1 N NaOH can be quantified from a maximum absorbance at 490 nm. Decarboxylated 6-aminofluorescein dissolved 6 N HCl (prepare by constant boiling at 110° C for 24 h) can be quantified from a maximum absorbance at 454 nm. Aldehyde groups are formed by oxidateive damage to proteins, which can be detected by conjugation to decarboxylated 6-aminofluorescein2.

参考文献