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62435-37-4

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62435-37-4 Usage

General Description

Methyl 4-N-octyloxybenzoate is a chemical compound commonly used in the production of various personal care and cosmetic products. It is often included in sunscreen, lotions, and moisturizers for its ability to absorb and reflect harmful ultraviolet rays. Methyl 4-N-octyloxybenzoate is classified as a benzoate ester and functions as an effective skin conditioning agent, providing hydration and protection from environmental stressors. It is also utilized as a fragrance ingredient in some products, enhancing their scent and appeal. This chemical has been deemed safe for use in limited concentrations and is regulated by various authorities to ensure its safety for consumer use.

Check Digit Verification of cas no

The CAS Registry Mumber 62435-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,3 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62435-37:
(7*6)+(6*2)+(5*4)+(4*3)+(3*5)+(2*3)+(1*7)=114
114 % 10 = 4
So 62435-37-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H24O3/c1-3-4-5-6-7-8-13-19-15-11-9-14(10-12-15)16(17)18-2/h9-12H,3-8,13H2,1-2H3

62435-37-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A10554)  Methyl 4-n-octyloxybenzoate, 98%   

  • 62435-37-4

  • 10g

  • 263.0CNY

  • Detail
  • Alfa Aesar

  • (A10554)  Methyl 4-n-octyloxybenzoate, 98%   

  • 62435-37-4

  • 50g

  • 1158.0CNY

  • Detail

62435-37-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL 4-N-OCTYLOXYBENZOATE

1.2 Other means of identification

Product number -
Other names methyl 4-octoxybenzoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62435-37-4 SDS

62435-37-4Relevant articles and documents

“Effect of the linking unit on the calamitic-shaped liquid crystal: a comparative study of two homologous series of benzoate and cinnamate linked compounds”

Kashyap, Dinesh,Patel, Sunil,Prajapat, Varsha,Sharma, Vinay,Vasava, Dilip

, p. 58 - 70 (2019/08/28)

Two homologous series based on three linking groups have been synthesized and well characterized by elemental analyses and spectroscopic techniques such as Fourier transform infrared [FT-IR] and proton magnetic resonance magnetic resonance [1H NMR] spectroscopy. The mesomorphic properties of these compounds were observed by using optical polarized microscopy (POM) and confirmed by differential scanning calorimetry (DSC) analysis. In this present investigation, we have synthesized two homologous series viz. (E)-4-(3-(4-(tetra decanoyloxy) phenyl) acryloyl) phenyl-4-n-alkoxy benzoate (Series-1) and 4-((E)-3-(4-(((E)-3-(4-n-alkoxy phenyl) acryloyl) oxy) phenyl)-3-oxo prop-1-en-1-yl) phenyl tetradecanoate (Series-2). Both of the series are differing with respect to the first linking group. All the homologous in following series displays LC properties on heating as well as cooling condition except first four homologous (C1 to C4) in series-1 and six homologous (C1 to C6) in series-2. To get more insights, the HOMO, LUMO studies are carried out which supports intramolecular charge transfer interactions in this class of mesogens.

New chalcone based liquid crystals with allylidene amino linking unit: Synthesis and characterization

Sharma, Vinay S.,Sharma, Anuj S.,Jadeja, Upendra H.,Suthar, Deepak

, p. 64 - 81 (2019/02/24)

In this study, the synthesis, structural characterization and mesomorphic properties of newly thirteen calamitic shaped compounds derived from allylidene amino chalcone and 4-n-alkoxy benzoyloxy benzoic acid. Comp.H1 to H3 exhibited nonliquid crystalline nature, while comp.H4 to comp.H18 displayed enantiotropical smectic C phase. Phase transition temperatures of present synthesised compounds were determined by optical polarising microscopy (POM), differential scanning calorimetric (DSC) and powder X-ray diffraction (PXRD) techniques. Thermal stabilities of smectic to isotropic phase are 150.0 °C and temperature range of mesophase is in decreasing order from comp.H3 to comp.H18 respectively. The presences of SmC phase are the type of broken fan and needle type in present synthesized series. It is also shown that presence of chalcone amino allylidene central linking group favors a calamitic liquid crystalline behaviour in molecules with lower member to higher member aliphatic side chain in alkoxy group (-OR).

Synthesis, characterization, crystal structure and liquid crystal studies of some symmetric naphthalene derivative molecules

Srinivasa,Palakshamurthy,Devarajegowda,Hariprasad

, p. 620 - 626 (2018/09/18)

The synthesis of a series of symmetrical liquid crystals having naphthalene as the central rigid core and attached to long chain flexible 4′-alkoxybenzoate moiety at positions 2,6 - of the aromatic ring are reported. The mesophase behavior of the molecules was investigated using differential scanning calorimetry (DSC), polarizing optical microscopy (POM) and X-ray diffraction studies. The studies reveal that the synthesized compounds exhibit stable enantiotropic mesophase of Smectic A (SmA) and Nematic (N) phase. The mesophase appearance is independent of the length of the alkyl chain. The molecular structure was determined by single crystal X-ray diffraction technique. The derivative with n-heptyloxy- flexible chain crystallizes under triclinic, P1ˉspace group with unit cell dimension a = 5.569(3) ? b = 10.540(5) ? c = 15.254(9) ? α = 73.434(18)o, β = 80.807(19)o and γ = 82.02(2)o, V = 843.1(8) ?3. The dihedral angle between the naphthalene ring system and the benzoate moiety is 63.63(2)o.

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