Welcome to LookChem.com Sign In|Join Free

Cas Database

57-10-3

57-10-3

Identification

  • Product Name:Palmitic acid

  • CAS Number: 57-10-3

  • EINECS:200-312-9

  • Molecular Weight:256.429

  • Molecular Formula: C16H32O2

  • HS Code:29157015

  • Mol File:57-10-3.mol

Synonyms:Palmiticacid (7CI,8CI);1-Pentadecanecarboxylic acid;Cetylic acid;Edenor C16;Emersol 143;FA 1695;Hydrofol Acid 1690;Hystrene 9016;Kortacid 1695;Kortacid 1698;Loxiol EP 278;Lunac P 95;Lunac P 95KC;Lunac P 98;NAA 160;NSC 5030;Neo-Fat 16;PA 900;Pentadecanecarboxylic acid;Prifac 2960;Pristerene 4934;V 1695;n-Hexadecanoic acid;n-Hexadecoic acid;

Post Buying Request Now
Entrust LookChem procurement to find high-quality suppliers faster

Safety information and MSDS view more

  • Pictogram(s):IrritantXi

  • Hazard Codes:Xi

  • Signal Word:No signal word.

  • Hazard Statement:none

  • First-aid measures: General adviceConsult a physician. Show this safety data sheet to the doctor in attendance.If inhaled Fresh air, rest. In case of skin contact Wash off with soap and plenty of water. Consult a physician. In case of eye contact First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention. If swallowed Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician. /SRP:/ Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand-valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. /Organic acids and related compounds/

  • Fire-fighting measures: Suitable extinguishing media Use water spray, powder, foam, carbon dioxide. Wear self-contained breathing apparatus for firefighting if necessary.

  • Accidental release measures: Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. For personal protection see section 8. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Pick up and arrange disposal. Sweep up and shovel. Keep in suitable, closed containers for disposal.

  • Handling and storage: Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Avoid exposure - obtain special instructions before use.Provide appropriate exhaust ventilation at places where dust is formed. For precautions see section 2.2. Separated from bases, oxidants and reducing agents. Well closed.

  • Exposure controls/personal protection:Occupational Exposure limit valuesBiological limit values Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday. Eye/face protection Safety glasses with side-shields conforming to EN166. Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU). Skin protection Wear impervious clothing. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace. Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique(without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it. Respiratory protection Wear dust mask when handling large quantities. Thermal hazards

Supplier and reference price

  • Manufacture/Brand
  • Product Description
  • Packaging
  • Price
  • Delivery
  • Purchase
  • Manufacture/Brand:Usbiological
  • Product Description:Palmitic Acid
  • Packaging:250g
  • Price:$ 368
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:TRC
  • Product Description:Palmitic acid
  • Packaging:10g
  • Price:$ 50
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:TCI Chemical
  • Product Description:Palmitic Acid >97.0%(GC)(T)
  • Packaging:25g
  • Price:$ 17
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:TCI Chemical
  • Product Description:Palmitic Acid >97.0%(GC)(T)
  • Packaging:500g
  • Price:$ 28
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:TCI Chemical
  • Product Description:Palmitic Acid >99.5%(GC)
  • Packaging:5g
  • Price:$ 89
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Palmitic acid ≥99%
  • Packaging:25g
  • Price:$ 105
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Palmitic Acid
  • Packaging:25gm
  • Price:$ 124
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Palmitic acid natural, 98%, FG
  • Packaging:1 kg
  • Price:$ 113
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Palmitic acid ≥95%, FCC, FG
  • Packaging:10 kg
  • Price:$ 148
  • Delivery:In stock
  • Buy Now
  • Manufacture/Brand:Sigma-Aldrich
  • Product Description:Palmitic acid European Pharmacopoeia (EP) Reference Standard
  • Packaging:
  • Price:$ 190
  • Delivery:In stock
  • Buy Now

Relevant articles and documentsAll total 142 Articles be found

A fluorometric assay for lysosomal phospholipase A2 activity using fluorescence-labeled truncated oxidized phospholipid

Abe, Akira,Hiraoka, Miki,Shayman, James A.,Ohguro, Hiroshi

, p. 164 - 170 (2018)

Lysosomal phospholipase A2 (LPLA2) is a key enzyme involved in the homeostasis of cellular phospholipids. Recently, LPLA2 was reported to preferentially degrade some truncated oxidized phospholipids at the sn-1 position. A commercially available, truncated oxidized phospholipid conjugated with a fluorescent dye, 1-palmitoyl-2-glutaroyl-sn-glycero-3-phosphoethanolamine-N-[4-(dipyrrometheneboron difluoride) butanoyl] (PGPE-BODIPY), was used to develop a specific assay for this enzyme. When recombinant mouse LPLA2 was incubated with liposomes consisting of 1,2-O-octadecyl-sn-glycero-3-phosphocholine/PGPE-BODIPY under acidic conditions, PGPE-BODIPY was converted to palmitic acid and a polar BODIPY-product. After phase partitioning by chloroform/methanol, the polar BODIPY-product was recovered in the aqueous phase and identified as 1-lyso-PGPE-BODIPY. The formation of 1-lyso-PGPE-BODIPY was quantitatively determined by fluorescent measurements. The Km and Vmax values of the recombinant LPLA2 for PGPE-BODIPY were 5.64 μM and 20.7 μmol/min/mg protein, respectively. Detectable activity against PGPE-BODIPY was present in LPLA2 deficient mouse sera, but the deacylase activity was completely suppressed by treatment with 4-(2-aminoethyl)benzenesulfonyl fluoride (AEBSF). AEBSF had no effect on LPLA2 activity. The LPLA2 activity of mouse serum pre-treated with AEBSF was specifically and quantitatively determined by this assay method. The PGPE-BODIPY and AEBSF based LPLA2 assay is convenient and can be used to measure LPLA2 activity in a variety of biological specimens.

A new triterpenoid with antimicrobial activity from Anemone rivularis

Zhao, Chun-Chao,Shao, Jian-Hua,Fan, Ju-Di

, p. 803 - 805 (2012)

A new triterpene ester 1 and six known triterpenoids were isolated from Anemone rivularis by repeated column chromatography. Their structures were identified as olean-9(11),12-dien-3-O-palmitate (1), lupeol (2), betulin (3), betulic acid (4), oleanolic acid (5), ursolic acid (6), and β-amyrin (7) by spectral analysis and comparison with the published data. In addition, compound 1 was evaluated in vitro for its antimicrobial activity. It was found to exhibit moderate activity against the Gram-positive bacteria B. subtilis and S. aureus.

Synthesis and tissue biodistribution of [ω-11C]palmitic acid. A novel PET imaging agent for cardiac fatty acid metabolism

Buckman,VanBrocklin,Dence,Bergmann,Welch,Katzenellenbogen

, p. 2481 - 2485 (1994)

In order to diagnose patients with medium-chain acyl-CoA dehydrogenase deficiency with a noninvasive diagnostic technique such as positron emission tomography, we have developed a synthesis of [ω-11C]palmitic acid. The radiochemical synthesis was achieved by coupling an alkylfuran Grignard reagent (7) with [11C]methyl iodide, followed by rapid oxidative cleavage of the furan ring to the carboxylate using ruthenium tetraoxide. Tissue biodistribution studies in rats comparing [ω-11C]palmitic acid and [1- 11C]palmitic acid show that the %ID/g and %ID/organ in the heart tissue after administration of [ω-11C]palmitic acid is approximately 50% greater than after administration of [1-11C]palmitic acid, due to the diminished metabolism of the [ω-11C]palmitic acid. These studies show as well, low uptake in nontarget tissues (blood, lung, kidney, and muscle). PET images of a dog heart obtained after administration of [ω-11C] and [1- 11C]palmitic acid show virtually identical uptake and distribution in the myocardium. The differing cardiac washout of labeled palmitates measured by dynamic PET studies may allow diagnosis of disorders in cardiac fatty acid metabolism.

Shell-detachable nanoparticles based on a light-responsive amphiphile for enhanced siRNA delivery

Li, Hong-Jun,Wang, Hong-Xia,Sun, Chun-Yang,Du, Jin-Zhi,Wang, Jun

, p. 1961 - 1964 (2014)

Novel light-responsive nanoparticles based on an amphiphile with a single photolabile linker between its hydrophilic head and hydrophobic tail was developed for small interfering RNA (siRNA) delivery. Upon UV exposure, cleavage of the linkage resulted in rapid shell detachment of the nanoparticles, which facilitated siRNA release and enhanced gene silencing efficiency.

Anti-HIV1 Diterpenoids from Leaves and Twigs of Polyalthia sclerophylla

Saepou, Siriporn,Pohmakotr, Manat,Reutrakul, Vichai,Yoosook, Chalobon,Kasisit, Jitra,Napaswad, Chanita,Tuchinda, Patoomratana

, p. 721 - 725 (2010)

Bioassay-guided fractionation and purification of the anti-HIV-1-active MeOH extract from the leaves and twigs of Polyalthia sclerophylla led to the isolation of two new compounds, ent-kaur-sclerodimer (1) and cyclotucanol 3-palmitate (2), along with the known ent-kaur-16-en-19-oic acid (3), 15-hydroxy-ent-kaur-16-en-19-oic acid (4), 15-acetoxy-ent-kaur-16-en-19-oic acid (5), 15-oxo-ent-kaur-16-en-19-oic acid (6), 16,17-dihydroxy-ent-kauran-19-oic acid (7), 16-hydroxy-ent-kauran-19-oic acid (xylopic acid) (8), a pseudodimer (15-hydroxy-ent-kaur-16-en-19-oic acid/17-hydroxy-ent-kaur-15-en-19-oic acid) (9), ermanin, nicotiflorin, and allantoin. Among these isolates, compound 3 was the most active in both anti-syncytium (EC50 13.7μg/mL and selectivity index 3.1) and HIV-1 reverse transcriptase (IC50 34.1μg/mL) assays. Georg Thieme Verlag KG Stuttgart.

New diterpenoids from the roots of Euphorbia ebracteolata Hayata

Deng, Bin,Mu, Shu-Zhen,Zhang, Jian-Xin,Hao, Xiao-Jiang

, p. 1503 - 1509 (2010)

Three new diterpenoids, ingenol-5,20-O,O-isopropylidene-3-palmitate (1), ingenol-5,20-O,O-isopropylidene-3-myristinate (2) and 3,19-dihydroxy-1(10),15- rosadien-2-one (3), were isolated from the roots of Euphorbia ebracteolata Hayata. Their structures wer

Production of the anti-inflammatory compound 6-o-palmitoyl-3-O-β-D- glucopyranosylcampesterol by callus cultures of lopezia racemosa cav. (onagraceae)

Salinas, Roberta,Arellano-Garcia, Jesus,Perea-Arango, Irene,Alvarez, Laura,Garduno-Ramirez, Maria Luisa,Marquina, Silvia,Zamilpa, Alejandro,Castillo-Espana, Patricia

, p. 8679 - 8690 (2014)

Lopezia racemosa Cav. is a plant used in Mexican traditional medicine to heal inflammatory diseases. From this plant we isolated the novel compound 6-O-palmitoyl- 3-O-β-D-glucopyranosylcampesterol (1) and 6-O-palmitoyl-3-O-β-D-glucopyranosyl-β- sitosterol (2), previously reported to have cytotoxic activity on several cancer cell lines. We evaluated the anti-inflammatory activity of 1 in vivo by mouse ear edema induced with 12-O-tetradecanoylphorbol-13-acetate (TPA) and 57.14% inhibition was observed. The aim of our study was to obtain callus cultures derived from this plant species with the ability to produce the compounds of interest. Callus cultures were initiated on MS basal medium amended with variable amounts of naphthaleneacetic acid (NAA), or 2,4-dichlorophenoxyacetic acid (2,4-D), combined or not with 6-benzylaminopurine (BAP). Ten treatments with these growth regulators were carried out, using in vitro germinated seedlings as source of three different explants: hypocotyl, stem node, and leaf. Highest yield of 1 was observed on callus derived from leaf explants growing in medium containing 1.0 mg/L 2,4-D and 0.5 mg/L BAP. Selected callus lines produced less 1 than wild plants but the in vitro cultured seedlings showed higher production. So we conclude that it could be attractive to further investigate their metabolic potential.

Long-chain fatty acid acylated derivatives of isoflavone glycosides from the rhizomes of Iris domestica

Li, Jiayuan,Liu, Yanfei,Ni, Gang,Wang, Renzhong,Yu, Dequan

, (2021/11/01)

Six undescribed long-chain fatty acid esters of isoflavone glycosides were obtained from the rhizomes of Iris domestica (L.). Their structures were elucidated by comprehensive spectroscopic data, alkaline hydrolysis, and acid hydrolysis. This is the first report of the long-chain (C14–C18) fatty acid derivatives of isoflavone glycosides from natural products. Belamcandnoate B and D exhibited moderate cytotoxic activities against HCT-116, HepG2, and BGC823 cell lines with IC50 values of 1.69–6.86 μM. Belamcandnoate B and E exhibited 72.27 and 58.98% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM.

Biochemical and biophysical characterisation of a small purified lipase from Rhizopus oryzae ZAC3

Ayinla, Zainab A.,Ademakinwa, Adedeji N.,Gross, Richard A.,Agboola, Femi K.

, (2021/02/16)

The characteristics of a purified lipase from Rhizopus oryzae ZAC3 (RoL-ZAC3) were investigated. RoL-ZAC3, a 15.8 kDa protein, which was optimally active at pH 8 and 55 °C had a half-life of 126 min at 60 °C. The kinetic parameters using p-nitrophenylbuty

Lipase mimetic cyclodextrins

Lee, Youngjun,Devaraj, Neal K.

, p. 1090 - 1094 (2021/02/06)

Glycerophospholipids (GPLs) perform numerous essential functions in biology, including forming key structural components of cellular membranes and acting as secondary messengers in signaling pathways. Developing biomimetic molecular devices that can detect specific GPLs would enable modulation of GPL-related processes. However, the compositional diversity of GPLs, combined with their hydrophobic nature, has made it challenging to develop synthetic scaffolds that can react with specific lipid species. By taking advantage of the host-guest chemistry of cyclodextrins, we have engineered a molecular device that can selectively hydrolyze GPLs under physiologically relevant conditions. A chemically modified α-cyclodextrin bearing amine functional groups was shown to hydrolyze lyso-GPLs, generating free fatty acids. Lyso-GPLs are preferentially hydrolyzed when part of a mixture of GPL lipid species, and reaction efficiency was dependent on lyso-GPL chemical structure. These findings lay the groundwork for the development of molecular devices capable of specifically manipulating lipid-related processes in living systems.

Fabrication of dual catalytic microcapsules by mesoporous graphitic carbon nitride (mpg-C3N4) nanoparticle-enzyme conjugate stabilized emulsions

Varshney, Rohit,Kumar, Sushil,Ghosh, Kaushik,Patra, Debabrata

, p. 3097 - 3102 (2020/03/03)

Emulsionlated microcapsules (MCs) were fabricated by simultaneous self-assembly and crosslinking of mpg-C3N4 nanoparticles (NPs) and lipase conjugates at an oil-water interface. The presence of both enzymes and mpg-C3Nsub

Calixarenes functionalised water-soluble iron oxide magnetite nanoparticles for enzyme immobilisation

Sayin, Serkan,Ozyilmaz, Elif,Oguz, Mehmet,Yusufoglu, Rüstem,Yilmaz, Mustafa

, p. 334 - 344 (2020/03/30)

In this study, we first used water-soluble iron oxide nanoparticles for Candida rugosa lipase immobilisation. Moreover, two new complexation phenomena of the prepared water-soluble Fe3O4 nanoparticles with an enzyme might address int

Process route upstream and downstream products

Process route

4-nitrophenyl palmitate
1492-30-4

4-nitrophenyl palmitate

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

Conditions
Conditions Yield
With 4-(dialkylamino)pyridine linear oligomer (4) (n ca. 10); phosphate buffer pH 8.0; In methanol; at 30 ℃; Rate constant; other p-nitrophenyl alkanoates and 4-(dialkylamino)pyridines; dependence of reaction velocity on alkanoate chain length;
With N,N',N'',N'''-tetrakis-<10-decyl>-3,10,21,28-tetraoxo-2,11,20,29-tetra-aza<3.3.3.3>paracyclophane tetrachloride; In ethanol; water; at 30 ℃; Rate constant; other catalyst (three isomers containing two imidazolyl groups on adjacent and opposite alkyl chains); catalytic activity and substrate selectivity of both paracyclophanes compared; pH dependency of the substrate-binding ability of the cyclophanes;
With sodium hydrogencarbonate; sodium carbonate; In water; dimethyl sulfoxide; at 45 ℃; Rate constant; effect of DMSO ratio;
With water; In dimethyl sulfoxide; at 35 ℃; Kinetics; Thermodynamic data; pH=13.12; ΔH(excit.); -ΔS(excit.); different substrate concentrations, ratios of solvents, pHs and temperature;
With sodium phosphate buffer; Klebsiella sp. ZD112 pyrethroid-hydrolyzing esterase; In acetonitrile; at 30 ℃; pH=7.0; Enzyme kinetics;
With Penicillium expansum lipase; In water; at 37 ℃; pH-value; Solvent; Time; Concentration; Reagent/catalyst; Temperature; Kinetics; Ionic liquid; Enzymatic reaction;
With solid phase supported Thermomyces lanuginosus lipase; Triton X-100; In isopropyl alcohol; pH=7; aq. phosphate buffer; Enzymatic reaction;
With Burkholderia cepacia LTEB11 lipase; In isopropyl alcohol; pH=7; aq. phosphate buffer; Enzymatic reaction;
With Spirulina platensis lipase; In ethanol; at 45 ℃; for 0.1h; pH=6.5; Kinetics; aq. phosphate buffer; Enzymatic reaction;
With water; sodium cholate; Gum arabic; In isopropyl alcohol; at 20 ℃; for 4h; pH=7.8; Reagent/catalyst; Time; Concentration; Kinetics; aq. buffer; Enzymatic reaction;
With hydrogenchloride; recombinant Sulfolobus solfataricus P1 esterase; water; sodium taurocholate; 2-amino-2-hydroxymethyl-1,3-propanediol; at 60 ℃; pH=8.0; Kinetics; Enzymatic reaction;
With carboxylesterase EstSt7 from Sulfolobus tokodaii strain 7; water; In ethanol; at 80 ℃; pH=9; Kinetics; Enzymatic reaction;
With lipase from Pseudomonas stutzeri PS59; In aq. phosphate buffer; isopropyl alcohol; at 30 ℃; for 0.25h; pH=8.5; Solvent; Temperature; pH-value; Catalytic behavior; Enzymatic reaction;
With porcine pancreatic lipase; In aq. phosphate buffer; at 25 ℃; for 0.0666667h; pH=7.5; Reagent/catalyst; Kinetics; Enzymatic reaction;
With recombinant esterase from Rhizomucor miehei; In isopropyl alcohol; at 50 ℃; for 0.166667h; pH=7.5; Catalytic behavior; Enzymatic reaction;
With porcine pancreatic lipase-supported UiO-66(Zr) metal-organic framework; In aq. phosphate buffer; ethanol; at 20 ℃; for 0.0833333h; pH=7.2; Green chemistry; Enzymatic reaction;
With lipase-Cu3(PO4)2*3H2O nanoflower-PVA-chitosan composite; In aq. phosphate buffer; isopropyl alcohol; at 37 ℃; for 0.0833333h; pH=7.4; Reagent/catalyst; Kinetics; Enzymatic reaction;
With water; 2-amino-2-hydroxymethyl-1,3-propanediol; calcium chloride; In isopropyl alcohol; at 60 ℃; pH=7.4; Kinetics;
With sodium carbonate; In aq. phosphate buffer; isopropyl alcohol; at 20 ℃; for 0.0833333h; pH=7; Enzymatic reaction;
With water; Rhizopus oryzae ZAC3 lipase; In aq. phosphate buffer; isopropyl alcohol; pH=8; Enzymatic reaction;
1,2-dipalmitoyl-3-glyceryl p-nitrophenyl phosphate
189635-42-5

1,2-dipalmitoyl-3-glyceryl p-nitrophenyl phosphate

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

Conditions
Conditions Yield
With N,N,N'-Trimethyl-N'-hexadecylethylene diamine; water; uranyl ion; at 37 ℃; Rate constant; HEPES buffer, 0.01 M KCl, pH: 4.9;
vinyl palmitate
693-38-9

vinyl palmitate

glycerolcholine phosphate
34688-34-1,563-24-6

glycerolcholine phosphate

1,2-dipalmitoyl-rac-glycero-3-phosphatidylcholine
2644-64-6,2797-68-4

1,2-dipalmitoyl-rac-glycero-3-phosphatidylcholine

1-palmitoyllysophosphatidylcholine
17364-18-0

1-palmitoyllysophosphatidylcholine

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

Conditions
Conditions Yield
Lecitase surfactant-coated (modified)-immobilized enzyme complex on Duolite A568; In tert-butyl alcohol; at 60 ℃; for 72.5h; Enzyme kinetics; Enzymatic reaction;
benzyl arsonic acid
620-27-9

benzyl arsonic acid

n-hexadecanoyl chloride
112-67-4

n-hexadecanoyl chloride

C<sub>32</sub>H<sub>63</sub>AsO<sub>5</sub>

C32H63AsO5

benzyl chloride
100-44-7

benzyl chloride

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

benzyl alcohol
100-51-6,185532-71-2

benzyl alcohol

Conditions
Conditions Yield
With pyridine; In dichloromethane; for 576h; Product distribution; Ambient temperature; other time, other amounts of palmitoyl chloride and pyridine; also with palmitic anhydride, other alkylarsonic acid;
linseed oil

linseed oil

9-cis-13-trans-15-cis-octadecatrienoic acid

9-cis-13-trans-15-cis-octadecatrienoic acid

9,11,13-octadecatrienoic acid
13296-76-9

9,11,13-octadecatrienoic acid

10,12,14-C<sub>18</sub>:3
104096-79-9

10,12,14-C18:3

10E,12Z,14E-C<sub>18</sub>:3
25574-96-3

10E,12Z,14E-C18:3

cis-Octadecenoic acid
112-80-1,2027-47-6

cis-Octadecenoic acid

cis-9,trans-11-octadecadienoic acid
544-70-7,544-71-8,872-23-1,1839-11-8,2540-56-9

cis-9,trans-11-octadecadienoic acid

trans-10,cis-12-octadecadienoic acid
1072-36-2,2420-44-2,2420-56-6,7307-45-1,22880-03-1

trans-10,cis-12-octadecadienoic acid

cis-vaccenic acid
506-17-2

cis-vaccenic acid

(9Z,12Z,15Z)-octadeca-9-12,15-trienoic acid
463-40-1,1955-33-5,21661-10-9,21661-09-6,21661-13-2,21661-11-0

(9Z,12Z,15Z)-octadeca-9-12,15-trienoic acid

9-(6-propyl-cyclohexa-2,4-dienyl)-nonanoic acid
25491-26-3

9-(6-propyl-cyclohexa-2,4-dienyl)-nonanoic acid

rumelenic acid
15909-18-9

rumelenic acid

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

stearic acid
57-11-4

stearic acid

Conditions
Conditions Yield
With sodium hydroxide; In propylene glycol; at 160 ℃; for 2h;
borage oil

borage oil

6Z,8E,12Z-C<sub>18</sub>:3
657403-47-9

6Z,8E,12Z-C18:3

7E,9Z,11E-C<sub>18</sub>:3

7E,9Z,11E-C18:3

cis-Δ9-docosenoic acid
25692-11-9,14134-53-3

cis-Δ9-docosenoic acid

cis-Octadecenoic acid
112-80-1,2027-47-6

cis-Octadecenoic acid

cis-9,trans-11-octadecadienoic acid
544-70-7,544-71-8,872-23-1,1839-11-8,2540-56-9

cis-9,trans-11-octadecadienoic acid

trans-10,cis-12-octadecadienoic acid
1072-36-2,2420-44-2,2420-56-6,7307-45-1,22880-03-1

trans-10,cis-12-octadecadienoic acid

cis-vaccenic acid
506-17-2

cis-vaccenic acid

gadoleic acid
29204-02-2,506-31-0

gadoleic acid

(9Z,12Z,15Z)-octadeca-9-12,15-trienoic acid
463-40-1,1955-33-5,21661-10-9,21661-09-6,21661-13-2,21661-11-0

(9Z,12Z,15Z)-octadeca-9-12,15-trienoic acid

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

stearic acid
57-11-4

stearic acid

(6Z,10E,12Z)-octadeca-6,10,12-trienoic acid
109241-60-3

(6Z,10E,12Z)-octadeca-6,10,12-trienoic acid

Conditions
Conditions Yield
With sodium hydroxide; In propylene glycol; at 160 ℃; for 2h;
cis-9-hexadecenoic acid
373-49-9,2091-29-4

cis-9-hexadecenoic acid

cis-Octadecenoic acid
112-80-1,2027-47-6

cis-Octadecenoic acid

Elaidic acid
112-79-8,2027-47-6

Elaidic acid

(9Z,12Z)-octadeca-9,11-dienoic acid
544-70-7

(9Z,12Z)-octadeca-9,11-dienoic acid

cis-9,trans-11-octadecadienoic acid
544-70-7,544-71-8,872-23-1,1839-11-8,2540-56-9

cis-9,trans-11-octadecadienoic acid

(10Z,12Z)-Octadeca-9,11-dienoic acid
7307-45-1

(10Z,12Z)-Octadeca-9,11-dienoic acid

trans-10,cis-12-octadecadienoic acid
1072-36-2,2420-44-2,2420-56-6,7307-45-1,22880-03-1

trans-10,cis-12-octadecadienoic acid

gadoleic acid
29204-02-2,506-31-0

gadoleic acid

Arachidic acid
506-30-9

Arachidic acid

n-docosanoic acid
112-85-6

n-docosanoic acid

n-tetradecanoic acid
544-63-8

n-tetradecanoic acid

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

stearic acid
57-11-4

stearic acid

octadeca-11Z,13Z-dienoic acid
117624-52-9

octadeca-11Z,13Z-dienoic acid

Conditions
Conditions Yield
With sodium hydroxide; ethanol; water; at 150 - 215 ℃; for 0 - 6h; under 7500.75 - 24002.4 Torr; Product distribution / selectivity;
With potassium hydroxide; ethanol; water; at 150 ℃; for 0 - 6h; under 7500.75 - 9000.9 Torr; Product distribution / selectivity;
With potassium hydroxide; water; In propylene glycol; at 150 ℃; for 0 - 6h; under 7500.75 - 9000.9 Torr; Product distribution / selectivity;
phenylacetic acid
103-82-2

phenylacetic acid

cis-Octadecenoic acid
112-80-1,2027-47-6

cis-Octadecenoic acid

2-phenylnaphthalene
612-94-2

2-phenylnaphthalene

1,4-diphenylbutane
1083-56-3

1,4-diphenylbutane

1-(naphthalen-2-yl)naphthalene
4325-74-0

1-(naphthalen-2-yl)naphthalene

1-phenylnaphthalene
605-02-7

1-phenylnaphthalene

1-phenyl-1,2,3,4-tetrahydronaphthalene
3018-20-0

1-phenyl-1,2,3,4-tetrahydronaphthalene

1-phenyl-1,2-dihydronaphtalene
16606-46-5

1-phenyl-1,2-dihydronaphtalene

1,7-diphenylnaphthalene
970-06-9

1,7-diphenylnaphthalene

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

Conditions
Conditions Yield
With aluminum tri-bromide; at 60 ℃; for 0.5h; Sonication;
1-Hexadecanol
36653-82-4,124-29-8

1-Hexadecanol

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

Conditions
Conditions Yield
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium chloride; oxygen; In 1,2-dichloro-ethane; at 25 ℃; for 12h; Time; Concentration; Reagent/catalyst;
99%
With hydrogenchloride; 2,2,6,6-tetramethyl-piperidine-N-oxyl; Amberlite IRA 900 chlorite; In dichloromethane; at 20 ℃; for 2h;
94%
With Cu(II)-complex of salen-H4; dihydrogen peroxide; In acetonitrile; at 80 ℃; for 9h;
90%
With Jones reagent; In acetone; at 0 ℃; for 1.5h;
73%
With potassium hydroxide; In 1,3,5-trimethyl-benzene; at 160 ℃; for 24h; Inert atmosphere;
60%
With dihydrogen peroxide; oxygen; (2-OPhCH2NHCH2)2(2-)*Co(2+); In acetonitrile; at 80 ℃; for 11h;
59%
With tert.-butylhydroperoxide; at 100 ℃; for 5h;
55%
With aluminum (III) chloride; Oxone; In water; at 60 ℃; for 8h;
36%
With chromic acid;
With potashlime; calcium carbonate; at 275 - 280 ℃;
With Jones reagent; In acetone; at 20 ℃;
p-methoxybenzyl palmitate

p-methoxybenzyl palmitate

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

Conditions
Conditions Yield
With oxalyl dichloride; In 1,2-dichloro-ethane; at 20 ℃; for 2.66667h;
97%
With trichlorophosphate; In 1,2-dichloro-ethane; at 20 ℃; for 1h;
92%
With iron(III) chloride; In dichloromethane; at 20 ℃; for 0.0833333h; Inert atmosphere; Green chemistry;
78%

Global suppliers and manufacturers

Global( 187) Suppliers
  • Company Name
  • Business Type
  • Contact Tel
  • Emails
  • Main Products
  • Country
  • Simagchem Corporation
  • Business Type:Manufacturers
  • Contact Tel:+86-592-2680277
  • Emails:sale@simagchem.com
  • Main Products:110
  • Country:China (Mainland)
  • Hangzhou Dingyan Chem Co., Ltd
  • Business Type:Manufacturers
  • Contact Tel:86-571-86465881,86-571-87157530,86-571-88025800
  • Emails:sales@dingyanchem.com
  • Main Products:95
  • Country:China (Mainland)
  • Chemwill Asia Co., Ltd.
  • Business Type:Manufacturers
  • Contact Tel:021-51086038
  • Emails:sales@chemwill.com
  • Main Products:30
  • Country:China (Mainland)
  • Shaanxi BLOOM TECH Co.,Ltd
  • Business Type:Lab/Research institutions
  • Contact Tel:+86-29-86470566
  • Emails:sales@bloomtechz.com
  • Main Products:80
  • Country:China (Mainland)
  • Shanghai Upbio Tech Co.,Ltd
  • Business Type:Lab/Research institutions
  • Contact Tel:+86-21-52196435
  • Emails:upbiocn@hotmail.com
  • Main Products:88
  • Country:China (Mainland)
close
Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 57-10-3
Post Buying Request Now
close
Remarks: The blank with*must be completed