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CAS RN: 150993-63-8 | 产品编码: A5564

(S)-(-)-DBD-Pro-COCl [=(S)-(-)-4-(N,N-Dimethylaminosulfonyl)-7-(2-chloroformylpyrrolidin-1-yl)-2,1,3-benzoxadiazole] [HPLC Labeling Reagent for e.e. Determination]


纯度/分析方法: >90.0%(HPLC)
别名:
  • (S)-(-)-DBD-Pro-COCl [=(S)-(-)-4-(N,N-二甲氨基磺酰基)-7-(2-氯甲酰四氢吡咯-1-基)-2,1,3-苯并恶二唑] [用于e.e.值测定的HPLC标记试剂]
  • (S)-(-)-4-(N,N-二甲基氨基磺酰)-7-(2-氯甲酰吡咯烷-1-基)苯并呋咱
  • (S)-(-)-4-(N,N-Dimethylaminosulfonyl)-7-(2-chloroformylpyrrolidin-1-yl)benzofurazan
  • (S)-(-)-4-(N,N-Dimethylaminosulfonyl)-7-(2-chloroformylpyrrolidin-1-yl)-2,1,3-benzoxadiazole
产品文档:
100MG
S$306.00
0   0   下单后约5-6个月内可以发货

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产品编码 A5564
纯度/分析方法 >90.0%(HPLC)
分子式/分子量 C__1__3H__1__5ClN__4O__4S = 358.80 
外观与形状(20°C) 固体
储存温度 冷藏 (0-10°C)
储存在惰性气体下 存放于惰性气体之中
应避免的情况 湿气 (分解),加热
包装和容器 100MG-Glass Bottle with Plastic Insert (查看图片)
CAS RN 150993-63-8
PubChem物质ID 87563181
MDL编号

MFCD00191380

技术规格
Appearance Light yellow to Yellow to Orange powder to crystal
Purity(HPLC) min. 90.0 area%
Optical purity(LC) min. 99.0 ee%
Effect test of HPLC derivatization Effective as labeling agent fo 2-Hexanol
Elemental analysis(Nitrogen) 15.00 to 16.00 %
NMR confirm to structure
物性(参考值)
GHS
象形图 Pictogram
信号词 Warning
危险性说明 H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
防范说明 P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P302 + P352 : IF ON SKIN: Wash with plenty of water.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
相关法规
运输信息
HS编码* 2935.90-000
*此H.S.编码用于日本出口报关,不适用于您所在国家或地区的进口申报
应用
HPLC Labeling Reagent for Chiral Alcohols and Amines

The compound 1 is an HPLC fluorescence labeling reagent for optical purity determination, which easily reacts with optical active alcohols or amines to form the corresponding esters or amides, respectively. The resultant esters or amides are stable and can reach the detector without any decomposition under reversed and normal phase HPLC. An excellent chromatogram can be obtained by fluorescence detection at the excitation and emission wavelengths of 450 nm and 560 nm, respectively. And the diastereomers derived from racemic alcohol and 1 can be separated by HPLC (The separation factor α: 2-hexanol = 1.2). Since no racemization can occur with derivatization reaction, it is possible to change an elution order of the labeled diastereomeres by selecting the enantiomer [(R)-(+)-DBD-Pro-COCl] of 1. The detection limit for the alcohols is sub-picomol. A highly sensitive analysis can be done by peroxyoxalate chemiluminescence detection.

Application example:
[Secondary alcohols] 1)
Add 1 mL of 10 mM labeling reagent 1 / dry benzene solution and 1 mL of 2 mM alcholol / dry benzene (containing 1% of pyridine) solution to a vessel. Close the cap of the reaction vessel and incubate the mixture at 80 °C for 3 h. After cooling to room temperature, excess of 1 is removed by liquid-liquid extraction (e.g. washing with 5% NaHCO3 solution) or solid phase extraction. Use the resultant as an HPLC sample solution.

References


参考文献


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