C99000
Cycloheptanone
99%
Synonym(s):
Ketocycloheptane, Ketoheptamethylene, Suberone
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About This Item
Linear Formula:
C7H12(=O)
CAS Number:
Molecular Weight:
112.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-937-6
Beilstein/REAXYS Number:
969823
MDL number:
Product Name
Cycloheptanone, 99%
form
liquid
InChI
1S/C7H12O/c8-7-5-3-1-2-4-6-7/h1-6H2
InChI key
CGZZMOTZOONQIA-UHFFFAOYSA-N
SMILES string
O=C1CCCCCC1
assay
99%
refractive index
n20/D 1.461 (lit.)
bp
179 °C (lit.)
density
0.951 g/mL at 25 °C (lit.)
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
131.0 °F
flash_point_c
55 °C
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Regulatory Information
危险化学品
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Brian T Sullivan et al.
Journal of chemical ecology, 47(1), 10-27 (2021-01-07)
We investigated geographic variation in the semiochemistry of major disturbance agents of western North American pine forests, Dendroctonus brevicomis Le Conte and Dendroctonus barberi Hopkins (Coleoptera: Curculionidae: Scolytinae), species separated by the Great Basin in the USA that until recently
K D Holland et al.
Molecular pharmacology, 37(1), 98-103 (1990-01-01)
The convulsant and/or anticonvulsant activity of unsubstituted and mono-alkyl-substituted cyclopentanones and cyclohexanones were examined by testing the ability of these compounds to produce seizures or to inhibit seizures induced by pentylenetetrazol and maximal electroshock in CF-1 mice. In addition, these
Khairia M Youssef et al.
Archiv der Pharmazie, 337(1), 42-54 (2004-02-05)
New series of 3, 5-bis(substituted benzylidene)-4-piperidones, 2, 7-bis(substituted benzylidene)cycloheptanones, 1, 5-bis(substituted phenyl)-1, 4-pentadien-3-ones, 1, 7-bis(substituted phenyl)-1, 6-heptadien-3, 5-diones, 1, 1-bis(substituted cinnamoyl)-cyclopentanes, and 1, 1-bis(substituted cinnamoyl)cyclohexanes have been synthesized and tested for their antioxidant activity. Among the tested compounds, compounds II(4)
Avidor Shulman et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 8(1), 229-239 (2002-02-02)
Antibody 38C2 efficiently catalyzes deuterium-exchange reactions at the alpha position of a variety of ketones and aldehydes, including substrates that have a variety of sensitive functional groups. In addition to the regio- and chemoselectivity of these reactions, the catalytic rates
M Juza
Journal of chromatography. A, 865(1-2), 35-49 (2000-02-16)
A binary test mixture consisting of cyclopentanone and cycloheptanone is used for the performance evaluation of a pilot-scale simulated moving bed unit. The involved adsorption equilibria and the kinetic behavior are discussed in detail. The results of the test runs
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