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3-Heptyl nitrate, also known as 1-nitro-3-heptyl, is an organic compound with the chemical formula C7H15NO3. It is a nitrate ester derived from heptanol, where the hydroxyl group is replaced by a nitrate group. This colorless liquid is characterized by its fruity odor and is used as a synthetic flavoring agent in the food and beverage industry. It is also employed as a fragrance component in various cosmetic and personal care products. Due to its potential to release nitric oxide, 3-heptyl nitrate has been studied for its vasodilatory effects, which could have implications in medical applications. However, it is important to note that the use of such chemicals in consumer products is regulated to ensure safety.

4459-12-5

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4459-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4459-12-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,5 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4459-12:
(6*4)+(5*4)+(4*5)+(3*9)+(2*1)+(1*2)=95
95 % 10 = 5
So 4459-12-5 is a valid CAS Registry Number.

4459-12-5Upstream product

4459-12-5Downstream Products

4459-12-5Relevant academic research and scientific papers

Facile access to nitroalkanes: Nitration of alkanes by selective C[sbnd]H nitration using metal nitrate, catalyzed by in-situ generated metal oxide

Li, Na,Mao, Liqiu,Peng, Haoyu,Peng, Ling,Yin, Dulin,You, Kuiyi,Zhong, Wenzhou

, (2020)

Direct C ? H functionalization of inactive alkanes is an important strategy to streamline the preparation of functional molecules. Herein, we describe an operationally simple and effective alkane C ? H nitration reaction to access versatile nitroalkanes without cleavage of the C ? C skeleton. Nontoxic and inexpensive metal nitrate (Fe(NO3)3·9H2O) plays a dual role as catalyst precursors as well as nitro sources for the transformation. Experimental evidence and theoretical modeling have shown the formation of iron oxide as a key catalytic species for the alkane C ? H and NO2 activation, which favors a stepwise radical mechanism with initial alkyl radical formation.

Alkyl nitrate, hydroxyalkyl nitrate, and hydroxycarbonyl formation from the NOx-air photooxidations of C5-C8 n-alkanes

Arey,Kwok,Atkinson,Aschmann,Atkinson,Kwok,Atkinson

, p. 1020 - 1027 (2001)

In the troposphere, alkanes present in the gas phase react mainly with the OH radical to form an alkyl radical. Products of the gas-phase reactions of OH radicals with the n-alkanes, n-pentane through n-octane at 298 ± 2 K and 1 atm of air were studied using GC with flame ionization detection, combined GC-MS, and in situ atmospheric pressure ionization tandem MS. The alkyl nitrate, hydroxyalkyl nitrate, and hydroxycarbonyl formation yields combined with the published carbonyl yields arising from alkoxy radical decomposition and reaction with O2, account for ~ 95, ~ 80, ~ 70, and ~ 55% of n-pentane, n-hexane, n-heptane, and n-octane (with NO), respectively. Hydroxyalkyl nitrate formation accounts for a few percent of the overall reaction products, and was consistently ~ 25% of the corresponding alkyl nitrate yields. Significant fractions of the atmospheric reaction products of ≥ C5 n-alkanes (and other alkanes whose intermediate alkoxy radicals can isomerize) were composed of hydroxycarbonyls and hydroxyalkyl nitrates, compound classes which are difficult to analyze under atmospheric conditions.

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