Cypermethrin | Solubility of Things

Identification

Molecular formula

C₂₂H₁₉ClN₂O₃

CAS number

52315-07-8

IUPAC name

[cyano-(3-phenoxyphenyl)methyl] 2-(4-chlorophenyl)-3-methyl-butanoate

State

Cypermethrin is typically found in solid form as a pure compound at room temperature, however it can be present as a liquid when mixed in formulations for use as an insecticide.

Melting point (Celsius)

60.00

Melting point (Kelvin)

333.15

Boiling point (Celsius)

220.00

Boiling point (Kelvin)

493.15

General information

Molecular weight

416.30g/mol

Molar mass

416.3030g/mol

Density

1.2400g/cm³

Appearence

Cypermethrin appears as a crystalline solid that is pale yellow in color. It can vary to a yellowish-brown liquid depending on formulation, as it is often used in diluted liquid forms for agricultural purposes.

Comment on solubility

Solubility of [cyano-(3-phenoxyphenyl)methyl] 2-(4-chlorophenyl)-3-methyl-butanoate

The solubility of the compound [cyano-(3-phenoxyphenyl)methyl] 2-(4-chlorophenyl)-3-methyl-butanoate (C₂₂H₁₉ClN₂O₃) can be influenced by several factors, including its molecular structure, polarity, and the presence of functional groups.

Key considerations include:

Polarity: The presence of polar functional groups, such as the cyano (–C≡N) and ester (–COO) moieties, typically enhances solubility in polar solvents like water and alcohols.
Hydrophobic characteristics: The phenyl rings contribute hydrophobic properties, which can decrease solubility in polar solvents but may increase compatibility with organic solvents.
Temperature effects: Generally, increased temperature can lead to improved solubility for most organic compounds. It is advisable to assess solubility at various temperatures.

As always, one must consider that solubility can vary widely based on the specific conditions and solvent used:

In polar solvents: The compound may exhibit significant solubility.
In non-polar solvents: Expect lower solubility due to the presence of aromatic structures.

In summary, the solubility profile of this compound is likely to be a balance between its hydrophilic and hydrophobic characteristics, making it important to conduct practical solubility tests under various conditions to ascertain its behavior in different environments.

Interesting facts

Interesting Facts About [cyano-(3-phenoxyphenyl)methyl] 2-(4-chlorophenyl)-3-methyl-butanoate

[cyano-(3-phenoxyphenyl)methyl] 2-(4-chlorophenyl)-3-methyl-butanoate is a fascinating compound that exemplifies the intricate world of organic chemistry. Here are some engaging insights:

Versatile Applications: This compound is often explored in pharmaceutical research due to its potential bioactive properties. Its unique structure allows it to interact with various biological targets.
Mechanism of Action: The presence of the cyano group can enhance the electrophilic properties of the compound, which may lead to interesting reactivity patterns, including nucleophilic reactions that are pivotal in drug development.
Chirality and Activity: The compound possesses several chiral centers, making stereochemistry a crucial element when studying its biological activity. As noted by many scientists, "The right chiral form can be the difference between a potent drug and an ineffective one."
Phenyl Groups: The incorporation of phenyl rings not only influences solubility but also affects the compound's overall conformational stability and electronic distribution, vital for molecular interactions.
Environmental Stability: Given its chlorinated component, this compound might also be subjected to studies regarding its environmental persistence and bioaccumulation, which are critical in assessing ecological impact.

This compound stands as a testament to the beauty and complexity found in organic molecular design. With ongoing research, its applications and influences in various fields, from medicinal chemistry to material science, continue to expand, promising exciting developments in the future.

Synonyms

fenvalerate

51630-58-1

Phenvalerate

Pydrin

Sumicidin

Belmark

Tirade

Agrofen

Aqmatrine

Fenaxin

Fenkill

Fenoxin

Phenoxin

Ectrin

Fenkem

Fenval

Furitrothion

Insectral

Sanmarton

Sumifleece

Sumipower

Sumitick

Sumkidin

Sumibac

Sumifly

Tribute

Evercide 2362

Gold crest tribute

Sumicidin 20E

Caswell No. 077A

Fenvalerate [BSI:ISO]

S-5602

Cyano(3-phenoxyphenyl)methyl 2-(4-chlorophenyl)-3-methylbutanoate

CCRIS 311

HSDB 6640

Fenvalerate [INN:BAN]

WL 43775

EPA Shaughnessy Code: 109301

alpha-Cyano-3-phenoxybenzyl alpha-(4-chlorophenyl)isovalerate

OMS-2000

EINECS 257-326-3

Acadrex (TN)

Asana

Fenvalerate (BAN)

4-Chloro-alpha-(1-methylethyl)benzeneacetic acid cyano(3-phenoxyphenyl)methyl ester

BRN 2025982

CHEBI:5014

SD 43775

AI3-29235

Z6MXZ39302

alpha-Cyano-3-phenoxybenzyl 2-(4-chlorophenyl)isovalerate

FENVALERATE [MI]

FENVALERATE [ISO]

Fenvalerate-(phenoxy-d5)

S 5602

FENVALERATE [HSDB]

FENVALERATE [IARC]

FENVALERATE [MART.]

(Cyano(3-phenoxyphenyl)methyl-4-chloro-alpha-(1-methylethyl)phenylacetate)

WL-43775

[(S)-cyano-(3-phenoxyphenyl)methyl] (2R)-2-(4-chlorophenyl)-3-methylbutanoate

alpha-Cyano-3-phenoxybenzyl alpha-isopropyl-4-chlorophenylacetate

alpha-Cyano-3-phenoxybenzyl-2-(4-chlorophenyl)-3-methylbutyrate

[cyano-(3-phenoxyphenyl)methyl] 2-(4-chlorophenyl)-3-methylbutanoate

DTXSID101017940

(+)-alpha-Cyano-3-phenoxybenzyl-(+)-alpha-(4-chlorophenyl)isovalerate

Cyano(3-phenoxyphenyl)methyl 4-chloro-alpha-(1-methylethyl)benzeneacetate

alpha-Cyano-(3-phenoxyphenyl)methyl-4-chloro-alpha-(1-methylethyl)benzeneacetate

MFCD00055324

Benzeneacetic acid, 4-chloro-.alpha.-(1-methylethyl)-, cyano(3-phenoxyphenyl)methyl ester

fenvalarate

Cyano(3-phenoxybenzyl)methyl 2-(4-chlorophenyl)-3-methylbutyrate

FENVALERATE (IARC)

Benzeneacetic acid, 4-chloro-alpha-(1-methylethyl)-, cyano(3-phenoxyphenyl)methyl ester

FENVALERATE (MART.)

a-Cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate

alpha-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutyrate

alpha-cyano-m-phenoxybenzyl 2-(p-chlorophenyl)-3-methylbutyrate

Fenvalerate .alpha.

cyano[3-(phenyloxy)phenyl]methyl 2-(4-chlorophenyl)-3-methylbutanoate

Cyano(3-phenoxyphenyl)methyl 4-chloro-a-(1-methylethyl)benzeneacetate, 9CI

Sumicidin A .alpha.

CYANO(3-PHENOXYPHENYL)METHYL 4-CHLORO-.ALPHA.-(1-METHYLETHYL)BENZENEACETATE

Fenvalerate A .alpha.

Benzeneacetic acid, 4-chloro-.alpha.-(1-methylethyl)-, cyano (3-phenoxyphenyl)methyl ester,(S-(R*,R*))-

S 5602 A .alpha.

fenvaierate

pyrid

Fenvalethrin

Fenvaleric acid

UNII-Z6MXZ39302

Fenvalerate solution

methyl (R)-4-((3S,5R,7R,8R,9S,10S,13R,14S,17R)-7-hydroxy-10,13-dimethyl-3-((4-((pyridin-3-ylmethyl)amino)butyl)amino)hexadecahydro-1H-cyclopenta(a)phenanthren-17-yl)pentanoate

methyl (R)-4-((3S,5R,7R,8R,9S,10S,13R,14S,17R)-7-hydroxy-10,13-dimethyl-3-((4-((pyridin-3-ylmethyl)amino)butyl)amino)hexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate

(+-)-Fenvalerate

Fenvalerate 10 microg/mL in Isooctane

Fenvalerate 100 microg/mL in Isooctane

Fenvalerate (Standard)

Fenvalerate, >=97%

alpha-cyano-3-phenoxybenzyl alpha-isopropyl-4-chlorophenyl acetate

(RS)-alpha-Cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutyrate

SCHEMBL26911

DTXCID30621

(S)-alpha-Cyano-3-phenoxybenzyl(S)-2-(4-chlorophenyl)isovalerate

Cyano(3-phenoxyphenyl)methyl 2-(4-chlorophenyl)-3-methylbutanoate #

BMK1-H10

CHEMBL492491

(S)-.alpha.-Cyano-3-phenoxybenzyl(S)-2-(4-chlorophenyl)-3-methylbutyrate

NIOSH/CY1576360

HY-B2006R

OMS-200

OMS2000

Cyano (3-phenoxybenzyl)-2-(4-chlorophenyl)-3-methylbutyrate

alpha-Cyano-3-phenoxybenzyl alpha-(4-chlorophenyl)-iso-valerate

HY-B2006

OMS 2000

HSCI1_000043

s5602

(RS)-alpha-Cyano-3-phenoxybenzyl (RS)-2-(4-chloro-phenyl)-3-methylbutyrate

AKOS015904814

FF23275

MSK20226-1000B

USEPA/OPP Pesticide Code: 109301

NCGC00163508-01

NCGC00163508-02

NCGC00163508-03

AC-22281

AS-49365

CS-0014107

CY15763600

Fenvalerate Solution in Acetone, 1000ug/mL

NS00099445

D07952

Fenvalerate, PESTANAL(R), analytical standard

H11436

EN300-1717625

Q412010

alphaCyano3phenoxybenzyl 2(4chlorophenyl)isovalerate

alphaCyano3phenoxybenzyl2(4chlorophenyl)3methylbutyrate

alphaCyano3phenoxybenzyl alpha(4chlorophenyl)isovalerate

Fenvalerate, certified reference material, TraceCERT(R)

alpha-cyano-3-phenoxybenzyl isopropyl-4-chlorophenylacetate

alphaCyano3phenoxybenzyl alphaisopropyl4chlorophenylacetate

Cyano(3phenoxybenzyl)methyl 2(4chlorophenyl)3methylbutyrate

(+)alphaCyano3phenoxybenzyl(+)alpha(4chlorophenyl)isovalerate

alpha-Cyano-3-phenoxy-benzyl alpha-(4-chlorophenyl)isovalerate

(Cyano(3phenoxyphenyl)methyl4chloroalpha(1methylethyl)phenylacetate)

alpha-cyano-3-phenoxy-benzyl 2-(p-chlorophenyl)-2-isopropyl-acetate

alpha-Cyano-3-phenoxy-benzyl alpha-isopropyl-4-chlorophenylacetate

alpha-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoate

Cyano(3phenoxyphenyl)methyl 4chloroalpha(1methylethyl)benzeneacetate

(+)Alpha-cyano-3-phenoxybenzyl-(+)-alpha-(4-chlorophenyl)isovalerate

alphaCyano(3phenoxyphenyl)methyl4chloroalpha(1methylethyl)benzeneacetate

(+-)-4-Chloro-alpha-(1-methylethyl)benzeneacetic acid cyano(3-phenoxyphenyl)methyl ester

(RS)-.ALPHA.-CYANO-3-PHENOXYBENZYL (RS)-2-(4-CHLORO-PHENYL)-3-METHYLBUTYRATE

4Chloroalpha(1methylethyl)benzeneacetic acid cyano(3phenoxyphenyl)methyl ester

Benzeneacetic acid, 4chloroalpha(1methylethyl), cyano(3phenoxyphenyl)methyl ester

Cyano(3-phenoxyphenyl)methyl ester, 4-chloro-alpha-(1-methylethyl)benzeneacetic acid

(.ALPHA.RS)-.ALPHA.-CYANO-3-PHENOXYBENZYL (2RS)-2-(4-CHLOROPHENYL)-3-METHYLBUTYRATE

110-167-2

4-Chloro-a-(1-methylethyl)benzeneacetic acid cyano(3-phenoxyphenyl)methyl ester;Agrofen;Aqmatrine

BENZENEACETIC ACID, 4-CHLORO-.alpha.-(1-METHYLETHYL)-, CYANO(3-PHENOXYPHENYL) METHYL ESTER

BENZENEACETIC ACID, 4-CHLORO-alpha-(1-METHYLETHYL)-, CYANO(3-PHENOXYPHENYL) METHYL ESTER

Benzeneacetic acid, 4-chloro-alpha-(1-methylethyl)-, cyano(3-phenoxyphenyl)methyl ester, (+-)-