4-Phenyl-2-butanone - 10mM in DMSO, high purity , CAS No.2550-26-7

  • 10mM in DMSO
Item Number
P422886
Grouped product items
SKUSizeAvailabilityPrice Qty
P422886-1ml
1ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$69.90

Basic Description

SynonymsBENZYLACETONE | 4-Phenylbutan-2-one | 2550-26-7 | 4-Phenyl-2-butanone | 2-Butanone, 4-phenyl- | 4-Penylbutan-2-one | 1-Phenyl-3-butanone | Methyl phenethyl ketone | Phenethyl methyl ketone | Methyl 2-phenylethyl ketone | Benzyl acetone | 4-Phenyl-butan-2-one | Methyl phenylethyl
Specifications & Purity10mM in DMSO
Storage TempStore at -80°C
Shipped InIce chest + Ice pads

Associated Targets(Human)

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Raji (5516 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Cruzipain (33337 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Corticium (78 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pythium (470 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
luxR HTH-type transcriptional regulator LuxR (29 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 4-phenylbutan-2-one
INCHI InChI=1S/C10H12O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3
InChi Key AKGGYBADQZYZPD-UHFFFAOYSA-N
Canonical SMILES CC(=O)CCC1=CC=CC=C1
Isomeric SMILES CC(=O)CCC1=CC=CC=C1
WGK Germany 1
RTECS EL9600000
PubChem CID 17355
Molecular Weight 148.2
Beilstein 1907123
Reaxy-Rn 1907123

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Chemical and Physical Properties

Refractive Index1.512
Flash Point(°F)221 °F
Flash Point(°C)105℃
Boil Point(°C)235°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

WGK Germany 1
RTECS EL9600000
Reaxy-Rn 1907123

Related Documents

Citations of This Product

1. Jun-Yu Liang, Zhi-Bo Hou, Hao-Shu Wu, Yue An, Ji Zhang, Jun-Long Wang, Chun-Yu He, Qing-Zheng Hou.  (2022)  Chemical constituents of essential oil extracted from Rhododendron anthopogonoides and its bioactivities against Tribolium castaneum and Ditylenchus destructor.  BIOCHEMICAL SYSTEMATICS AND ECOLOGY,  103  (104431).  [PMID:]
2. Xie Chao, Lin Longfei, Huang Liang, Wang Zixin, Jiang Zhiwei, Zhang Zehui, Han Buxing.  (2021)  Zn-Nx sites on N-doped carbon for aerobic oxidative cleavage and esterification of C(CO)-C bonds.  Nature Communications,  12  (1): (1-12).  [PMID:34376654]
3. Wu Hua-Lei, Zhang Jian-Dong, Zhang Chao-Feng, Fan Xiao-Jun, Chang Hong-Hong, Wei Wen-Long.  (2017)  Characterization of Four New Distinct ω-Transaminases from Pseudomonas putida NBRC 14164 for Kinetic Resolution of Racemic Amines and Amino Alcohols.  APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY,  181  (3): (972-985).  [PMID:27714638]

References

1. Jun-Yu Liang, Zhi-Bo Hou, Hao-Shu Wu, Yue An, Ji Zhang, Jun-Long Wang, Chun-Yu He, Qing-Zheng Hou.  (2022)  Chemical constituents of essential oil extracted from Rhododendron anthopogonoides and its bioactivities against Tribolium castaneum and Ditylenchus destructor.  BIOCHEMICAL SYSTEMATICS AND ECOLOGY,  103  (104431).  [PMID:]
2. Xie Chao, Lin Longfei, Huang Liang, Wang Zixin, Jiang Zhiwei, Zhang Zehui, Han Buxing.  (2021)  Zn-Nx sites on N-doped carbon for aerobic oxidative cleavage and esterification of C(CO)-C bonds.  Nature Communications,  12  (1): (1-12).  [PMID:34376654]
3. Wu Hua-Lei, Zhang Jian-Dong, Zhang Chao-Feng, Fan Xiao-Jun, Chang Hong-Hong, Wei Wen-Long.  (2017)  Characterization of Four New Distinct ω-Transaminases from Pseudomonas putida NBRC 14164 for Kinetic Resolution of Racemic Amines and Amino Alcohols.  APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY,  181  (3): (972-985).  [PMID:27714638]

Solution Calculators