Propoxur Solution in Methanol - 100μg/mL in methanol，Uncertainty：3% , CAS No.114-26-1

CAS: 114-26-1 Cat. No.: BWY359238 Summenformel: C₁₁H₁₅NO₃ Molekulargewicht: 209.24 Beilstein Registry Number: 1879891 EG-Nummer: 204-043-8

GRADE & PURITY 100μg/mL in methanol，Uncertainty：3%

Synonyms

propoxur|114-26-1|Baygon|2-Isopropoxyphenyl methylcarbamate|Aprocarb|Propoxure|Sendran|Propoxylor|Blattanex|Blattosep|Mrowkozol|Propotox|Suncide|Bolfo|Boruho|Brygou|2-Isopropoxyphenyl N-methylcarbamate|Dalf dust|Invisi-Gard|Arprocarb|Isocarb|Propyon|Rhode

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Synonyme

propoxur | 114-26-1 | Baygon | 2-Isopropoxyphenyl methylcarbamate | Aprocarb | Propoxure | Sendran | Propoxylor | Blattanex | Blattosep | Mrowkozol | Propotox | Suncide | Bolfo | Boruho | Brygou | 2-Isopropoxyphenyl N-methylcarbamate | Dalf dust | Invisi-Gard | Arprocarb | Isocarb | Propyon | Rhode

Spezifikationen & Reinheit

100μg/mL in methanol，Uncertainty：3%

Storage

Store at 2-8°C

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Namen und Kennungen

• Kanonisches Lächeln: CC(C)OC1=CC=CC=C1OC(=O)NC
• IUPAC Name: (2-propan-2-yloxyphenyl) N-methylcarbamate
• InChIKey: ISRUGXGCCGIOQO-UHFFFAOYSA-N
• INCHI: 1S/C11H15NO3/c1-8(2)14-9-6-4-5-7-10(9)15-11(13)12-3/h4-8H,1-3H3,(H,12,13)
• Isomere SMILES: CC(C)OC1=CC=CC=C1OC(=O)NC
• WGK Deutschland: 3
• RTECS: FC3150000
• UN-Nummer: 2757
• Verpackungsgruppe: I
• Molekulargewicht: 209.24
• Beilstein: 1879891
• Reaxy-Rn: 1879891
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1879891&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Phenol ethers

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Phenol ethers
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenol ethers
• Alternative Parents: Phenoxy compounds Alkyl aryl ethers Propargyl-type 1,3-dipolar organic compounds Carboximidic acids and derivatives Organopnictogen compounds Imines Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Carboximidic acid derivative - Ether - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organooxygen compound - Organonitrogen compound - Imine - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring.
• External Descriptors: Carbamate insecticides

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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ACHE Tclin Acetylcholinesterase (1 Activities)

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ACHE Tclin Acetylcholinesterase (18204 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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TP53 Tchem Cellular tumor antigen p53 (48468 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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GMNN Tbio Geminin (128009 Activities)

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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Faah Anandamide amidohydrolase (3907 Activities)

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Aedes aegypti (630 Activities)

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Musca domestica (713 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Blattella germanica (87 Activities)

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Laodelphax striatellus (278 Activities)

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Anopheles gambiae (126 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Schmelzpunkt (°C): 84-87°C
• Molekulargewicht: 209.240 g/mol
• XLogP3: 1.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 209.105 Da
• Monoisotopic Mass: 209.105 Da
• Topological Polar Surface Area: 47.600 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 206.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Häufig gestellte Fragen

How should this product be stored?

Store at 2–8 °C. Refrigerated storage is required to maintain the specified shelf life.

How is this product shipped?

This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 114-26-1, the molecular formula is C11H15NO3, and the molecular weight is 209.24 g/mol. InChIKey ISRUGXGCCGIOQO-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.