What is the 1-Dodecanal?

1-Dodecanal is colourless liquid, while it's Molecular Formula is C12H24O. colourless liquid Used in the Food Industry: 1-Dodecanal is used as a flavoring agent for its fruity, fatty odor, enhancing the taste and aroma of various food products. Used in Personal Care Products: 1-Dodecanal is used as a preservative due to its antimicrobial properties, helping to prevent the growth of microorganisms and extend the shelf life of personal care products. Used in Agriculture: 1-Dodecanal is used as a pesticide to control pests and protect crops, thanks to its ability to inhibit the growth of fungi and other microorganisms. Used in Pharmaceutical Applications: 1-Dodecanal is studied for its potential role in cancer treatment and its ability to inhibit the growth of fungi, making it a candidate for further research and development in the pharmaceutical industry.

What is the CAS number for 1-Dodecanal?

The CAS number of 1-Dodecanal is 112-54-9.

What is the 1-Dodecanal?

1-Dodecanal is colourless liquid, while it's Molecular Formula is C12H24O. colourless liquid Used in the Food Industry: 1-Dodecanal is used as a flavoring agent for its fruity, fatty odor, enhancing the taste and aroma of various food products. Used in Personal Care Products: 1-Dodecanal is used as a preservative due to its antimicrobial properties, helping to prevent the growth of microorganisms and extend the shelf life of personal care products. Used in Agriculture: 1-Dodecanal is used as a pesticide to control pests and protect crops, thanks to its ability to inhibit the growth of fungi and other microorganisms. Used in Pharmaceutical Applications: 1-Dodecanal is studied for its potential role in cancer treatment and its ability to inhibit the growth of fungi, making it a candidate for further research and development in the pharmaceutical industry.

What is the CAS number for 1-Dodecanal?

The CAS number of 1-Dodecanal is 112-54-9.

Detailed introduction

Reliable factory customized supply Dodecyl aldehyde 112-54-9

Molecular Formula:C12H24O
Molecular Weight:184.322
Appearance/Colour:colourless liquid
Vapor Pressure:0.0344mmHg at 25°C
Melting Point:12 °C
Refractive Index:1.432 - 1.438
Boiling Point:242.2 °C at 760 mmHg
Flash Point:102 °C
PSA：17.07000
Density:0.823 g/cm³
LogP:4.10620

1-Dodecanal(Cas 112-54-9) Usage

General Description

1-Dodecanal, also known as laurinaldehyde, is an organic compound that belongs to the class of aldehydes. It is a colorless to pale-yellow liquid with a fruity, fatty odor. 1-Dodecanal is found naturally in various essential oils, such as citrus oils, and it is commonly used as a flavoring agent in the food industry. It also has antimicrobial properties, making it useful as a preservative in personal care products and as a pesticide in agriculture. In addition, 1-Dodecanal has been studied for its potential pharmaceutical applications, including its role in cancer treatment and its ability to inhibit the growth of fungi. Nonetheless, like many aldehydes, 1-Dodecanal is also a skin and eye irritant, and prolonged exposure to high levels may cause adverse health effects.

InChI:InChI=1/C12H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h12H,2-11H2,1H3

112-54-9 Relevant articles

A new insight into the oxidation of cyclododecane with hydrogen peroxide in the presence of iron-substituted polyoxotungstates

Santos, Isabel C. M. S.,Sim?es, Mário M. Q.,Balula, M. Salete S.,Neves, M. Gra?a P. M. S.,Cavaleiro, José A. S.,Cavaleiro, Ana M. V.

, p. 1623 - 1626 (2008)

The catalytic homogeneous oxidation of c...

A useful and environmentally benign synthetic protocol for dethiolization by employing vanadium pentoxide catalyzed oxidation of ammonium bromide by hydrogen peroxide

Mondal, Ejabul,Bose, Gopal,Sahu, Priti Rani,Khan, Abu T.

, p. 1158 - 1159 (2001)

A wide variety of thioacetals and thioke...

Conversion of Ketals to Ketones by Nitrogen Dioxide in the Presence of Silica Gel

Nishiguchi, Takeshi,Ohosima, Tatsuya,Nishida, Akiko,Fujisaki, Shizuo

, p. 1121 - 1122 (1995)

Nitrogen dioxide transforms ketals to ke...

A highly efficient procedure for regeneration of carbonyl groups from their corresponding oxathioacetals and dithioacetals using sodium nitrite and acetyl chloride in dichloromethane

Khan, Abu T.,Mondal, Ejabul,Sahu, Priti R.

, p. 377 - 381 (2003)

A wide variety of oxathioacetals 1 as we...

Dynamic Imine Chemistry at Complex Double Emulsion Interfaces

Zentner, Cassandra A.,Anson, Francesca,Thayumanavan,Swager, Timothy M.

, p. 18048 - 18055 (2019)

Interfacial chemistry provides an opport...

An expedient and efficient method for the cleavage of dithioacetals to the corresponding carbonyl compounds using organic ammonium tribromide (OATB)

Mondal,Bose,Khan

, p. 785 - 786 (2001)

A variety of dithioacetals of aldehydes ...

Sex pheromone and related compounds in the Ishigaki and Okinawa strains of the tussock moth Orgyia postica (Walker) (Lepidoptera: Lymantriidae)

Wakamura, Sadao,Arakaki, Norio,Yamamoto, Masanobu,Hiradate, Syuntaro,Yasui, Hiroe,Kinjo, Kunio,Yasuda, Tetsuya,Yamazawa, Hiroyuki,Ando, Tetsu

, p. 957 - 965 (2005)

Two distinct electroantennographycally a...

-

Damico,R.,Broaddus,C.D.

, p. 1607 - 1612 (1966)

Enolate and Other Carbon Nucleophile Alkylation Reactions Using 1,2-Cyclic Sulfates as Terminal Epoxide Equivalents

Hoye, Thomas R.,Crawford, Khushrav B.

, p. 520 - 522 (1994)

Enolates of esters and amides as well as...

Kinetics of the MnO4- oxidation of anionic surfactant (sodiumdodecyl sulphate): Evidence for the formation of soluble colloidal MnO2

Raju,Khan, Zaheer

, p. 1218 - 1222 (2005)

A conventional spectrophotometric techni...

Pyridinium poly(hydrogen fluoride)-assisted cleavage of acetals and ketals

Watanabe, Yutaka,Kiyosawa, Youko,Tatsukawa, Akiko,Hayashi, Minoru

, p. 4641 - 4643 (2001)

Acetals, including ketals, were smoothly...

Highly Selective Conversion of Terminal Olefins into Aldehydes

Brown, Herbert C.,Kulkarni, Surendra U.,Rao, C. Gundu

, p. 151 - 153 (1980)

Discovery of Anti-TNBC Agents Targeting PTP1B: Total Synthesis, Structure-Activity Relationship, in Vitro and in Vivo Investigations of Jamunones

Hu, Caijuan,Li, Guoxun,Mu, Yu,Wu, Wenxi,Cao, Bixuan,Wang, Zixuan,Yu, Hainan,Guan, Peipei,Han, Li,Li, Liya,Huang, Xueshi

, p. 6008 - 6020 (2021/05/06)

Twenty-three natural jamunone analogues ...

Cassis and Green Tea: Spontaneous Release of Natural Aroma Compounds from β-Alkylthioalkanones

B?ttig, Sarah,Bochet, Christian G.,Egger, Timothy,Flachsmann, Felix,Gey, Olga

, (2021/10/19)

In depth headspace analysis of the slow ...

Selective Production of Linear Aldehydes and Alcohols from Alkenes using Formic Acid as Syngas Surrogate

Chen, Junjun,Hua, Kaimin,Liu, Xiaofang,Deng, Yuchao,Wei, Baiyin,Wang, Hui,Sun, Yuhan

, p. 9919 - 9924 (2021/05/31)

Performing carbonylation without the use...

A Strategy for Accessing Aldehydes via Palladium-Catalyzed C?O/C?N Bond Cleavage in the Presence of Hydrosilanes

He, Zhanyu,Liu, Tingting,Ru, Junxiang,Wang, Yulin,Wang, Zijia,Zeng, Zhuo

, p. 5794 - 5800 (2020/12/01)

We report the catalytic reduction of bot...

112-54-9 Process route

: 18526-20-0
4-Dodecylsulfanyl-butan-2-one

: 625-34-3
3-oxobutyraldehyde

: 112-54-9
Dodecanal

: 34619-12-0
4-Mercapto-2-butanone

: 78-94-4,25038-87-3
methyl vinyl ketone

Conditions

Conditions	Yield
With air; at 20 ℃;

: trans-3-(dodecanylthio)-1-(2,6,6-trimethyl-3-cyclohexen-1-yl)-1-butanone

: 57378-68-4,41436-42-4,71048-82-3
1-(2,6,6-trimethyl-cyclohex-3-enyl)-but-2-en-1-one

: 112-54-9
Dodecanal

: 1-(2,6,6-trimethyl-3-cyclohexenyl)-1,3-butanedione

: C₁₃H₂₂OS