추천 제품
Grade
technical grade
Quality Level
분석
90%
형태
solid
bp
158-162 °C/9 mmHg (lit.)
mp
35-37 °C (lit.)
density
1.059 g/mL at 25 °C (lit.)
작용기
carboxylic acid
ketone
SMILES string
CC(=O)CCCCC(O)=O
InChI
1S/C7H12O3/c1-6(8)4-2-3-5-7(9)10/h2-5H2,1H3,(H,9,10)
InChI key
IZOQMUVIDMLRDC-UHFFFAOYSA-N
관련 카테고리
일반 설명
6-Oxoheptanoic acid is a monocarboxylic acid with acyl functional group. Mass spectrometric characterization of 6-oxoheptanoic acid by electrospray ionization coupled to a triple quadrupole and TOF analyzer hybrid system has been reported.
애플리케이션
6-Oxoheptanoic acid may be used in the following studies:
- As ketone linker used for the conjugation of hydrazide derivatives to proteins.
- Synthesis of N-(2-propynyl)-6-oxoheptanamide.
- Synthesis of adenosine triphosphate derivative.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
235.4 °F - closed cup
Flash Point (°C)
113 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Mass spectrometric characterization of small oxocarboxylic acids and gas phase ion fragmentation mechanisms studied by electrospray triple quadrupole-MS/MS-TOF system and DFT theory.
Kanawati B, et al.
International Journal of Mass Spectrometry, 266(1), 97-113 (2007)
A Safavy et al.
Bioconjugate chemistry, 10(1), 18-23 (1999-01-20)
A procedure utilizing an activated ester approach for conjugation of unprotected hydroxamic acids to antibodies and peptides was recently reported. Here, an alternative method with advantages over the activated ester strategy is described. This protocol utilizes the hydrazone formation between
Synthesis of methylketone containing nucleoside triphosphates for RNA labelling
Trevisiol E, et al.
Tetrahedron, 56(35), 6501-6510 (2000)
Erik Selander et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(20), 6395-6400 (2015-04-29)
Interactions among microscopic planktonic organisms underpin the functioning of open ocean ecosystems. With few exceptions, these organisms lack advanced eyes and thus rely largely on chemical sensing to perceive their surroundings. However, few of the signaling molecules involved in interactions
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