<Suppliers Price>

6-Oxoheptanoic acid

Names

[ CAS No. ]:
3128-07-2

[ Name ]:
6-Oxoheptanoic acid

[Synonym ]:
6-Oxoheptanoic acid
EINECS 221-512-2
5-aceto valeric acid
Heptanoic acid,6-oxo
6-oxyheptanoic acid
6-oxo-heptanoic acid
6-Oxoenanthic acid
5-Acetylpentanoic acid
Heptanoic acid, 6-oxo-
5-Acetylvaleric Acid
6-ketoheptanoic acid
MFCD00051479

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
299.3±23.0 °C at 760 mmHg

[ Melting Point ]:
35-37 °C(lit.)

[ Molecular Formula ]:
C7H12O3

[ Molecular Weight ]:
144.168

[ Flash Point ]:
149.1±19.1 °C

[ Exact Mass ]:
144.078644

[ PSA ]:
54.37000

[ LogP ]:
0.17

[ Vapour Pressure ]:
0.0±1.3 mmHg at 25°C

[ Index of Refraction ]:
1.444

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C: Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2918300090

Synthetic Route

Customs

[ HS Code ]: 2918300090

[ Summary ]:
2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Predator lipids induce paralytic shellfish toxins in bloom-forming algae.

Proc. Natl. Acad. Sci. U. S. A. 112 , 6395-400, (2015)

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...

Further studies on the protein conjugation of hydroxamic acid bifunctional chelating agents: group-specific conjugation at two different loci.

Bioconjug. Chem. 10(1) , 18-23, (1999)

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...

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.

Int. J. Mass Spectrom. 266(1) , 97-113, (2007)


More Articles


Related Compounds