38289-46-2 Usage
Description
4-N-NONYLBENZOIC ACID, also known as 4-Nonylbenzoic acid, is an organic compound with the molecular formula C16H24O2. It is a derivative of benzoic acid, featuring a nonyl group attached to the 4-position of the benzene ring. 4-N-NONYLBENZOIC ACID is characterized by its ability to retain perfume fragrance, making it a valuable component in various applications.
Uses
Used in Detergent Industry:
4-N-NONYLBENZOIC ACID is used as a bleaching agent for detergents, enhancing the cleaning power and whitening effect of the product. Its ability to retain perfume fragrance makes it a preferred choice for creating detergents with a pleasant scent that lasts longer.
Used in Perfumery:
In the perfume industry, 4-N-NONYLBENZOIC ACID is utilized as a fixative agent to prolong the longevity of fragrances in perfumes and other scented products. Its capacity to retain the scent of perfumes makes it an essential component in the formulation of long-lasting fragrances.
Used in Cosmetics:
4-N-NONYLBENZOIC ACID is also employed in the cosmetics industry, where it serves as an ingredient in various cosmetic products. Its fragrance retention properties contribute to the pleasant scent of these products, while its compatibility with other ingredients makes it a versatile component in the formulation of cosmetics.
Check Digit Verification of cas no
The CAS Registry Mumber 38289-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,8 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38289-46:
(7*3)+(6*8)+(5*2)+(4*8)+(3*9)+(2*4)+(1*6)=152
152 % 10 = 2
So 38289-46-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H24O2/c1-2-3-4-5-6-7-8-9-14-10-12-15(13-11-14)16(17)18/h10-13H,2-9H2,1H3,(H,17,18)
38289-46-2Relevant articles and documents
Potentiation of the fosmidomycin analogue FR 900098 with substituted 2-oxazolines against Francisella novicida
Stephens, Matthew D.,Yodsanit, Nisakorn,Melander, Christian
supporting information, p. 1952 - 1956 (2016/10/22)
A library of 33 compounds was screened for potentiation of the antibiotic FR 900098 against the Francisella tularensis surrogate Francisella novicida. From the screen a highly potent 2-oxazoline adjuvant was discovered capable of potentiating FR 900098 with a 1000-fold reduction in MIC against the Francisella sub-species F. novicida and F. philomiragia.
4-Nonylbenzoic acid: (Benzoic acid, 4-nonyl-)
Fürstner, Alois,Leitner, Andreas,Seidel, Günter,Kontnik, Renee,Wolff, Steven
, p. 33 - 41 (2017/09/30)
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New potent antagonists of leukotrienes C4 and D4. 1. Synthesis and structure-activity relationships
Nakai,Konno,Kosuge,Sakuyama,Toda,Arai,Obata,Katsube,Miyamoto,Okegawa,Kawasaki
, p. 84 - 91 (2007/10/02)
(p-Amylcinnamoyl)anthranilic acid (3a) had moderate antagonist activities against LTD4-induced smooth muscle contraction on guinea pig ileum and LTC4-induced bronchoconstriction in anesthetized guinea pigs. Modifications were made in the hydrophobic part (cinnamoyl moiety) and the hydrophilic part (anthranilate moiety) of 3a. A series of 8-(benzoylamino)-2-tetrazol-5-yl-1,4-benzodioxans and 8-(benzoylamino)-2-tetrazol-5-yl-4-oxo-4H-1-benzopyrans were revealed to be potent antagonists of leukotrienes C4 and D4. Among both series, ONO-RS-347 (18k) and ONO-RS411 (19h) were the most potent and orally active antagonists, respectively. Structure-activity relationships are discussed.
