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Merck
CN

87851

Supelco

2,2,6,6-四甲基-3,5-庚二酮

LiChropur, ≥98.0%

别名:

二叔戊酰甲烷

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About This Item

线性分子式:
(CH3)3CCOCH2COC(CH3)3
CAS Number:
分子量:
184.28
Beilstein:
1447269
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:

等级

derivatization grade ((GC derivatization))

质量水平

方案

≥98.0% (GC)
≥98.0%

表单

liquid

质量

LiChropur

反应适用性

reagent type: derivatization reagent
reaction type: Acylations

折射率

n20/D 1.456-1.462
n20/D 1.459 (lit.)

沸点

72-73 °C/6 mmHg (lit.)

密度

0.883 g/mL at 25 °C (lit.)

SMILES字符串

CC(C)(C)C(=O)CC(=O)C(C)(C)C

InChI

1S/C11H20O2/c1-10(2,3)8(12)7-9(13)11(4,5)6/h7H2,1-6H3

InChI key

YRAJNWYBUCUFBD-UHFFFAOYSA-N

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一般描述

Acylation, a replacement to silylation, allows the conversion of compounds that consist of active hydrogens (-OH, -SH and -NH) into esters, thioesters, and amides via the action of a carboxylic acid or derivative. The carbonyl group adjacent to the halogenated carbons is known to improve the electron capture detector (ECD) response. Acylation has several advantages:
  • It enhances the stability of compounds by protecting unstable groups.
  • It may confer volatility on substances like carbohydrates or amino acids, that have several polar groups that they are non-volatile and usually decompose on heating.
  • It facilitates the separations not possible with underivatized compounds.
  • Compounds are detectable at very low levels with an ECD.

2,2,6,6-Tetramethyl-3,5-heptanedione is a reagent used to form fragmentation-directing derivatives for GC/MS analysis.

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法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

152.6 °F - closed cup

闪点(°C)

67 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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