Amyl lactate

Base Information

• Chemical Name: Amyl lactate
• CAS No.: 6382-06-5
• Molecular Formula: C8H16O3
• Molecular Weight: 160.213
• European Community (EC) Number: 228-974-4
• NSC Number: 406253
• UNII: N3400NO5KU
• DSSTox Substance ID: DTXSID70858752
• Nikkaji Number: J113.001C
• Wikidata: Q27284472
• Mol file: 6382-06-5.mol

Synonyms:Amyl lactate;Pentyl lactate;Pentyl 2-hydroxypropanoate;6382-06-5;Lactic acid, pentyl ester;Propanoic acid, 2-hydroxy-, pentyl ester;n-Amyl lactate;N3400NO5KU;NSC-406253;amyllactat;n-pentyl lactate;pentyl DL-lactate;UNII-N3400NO5KU;SCHEMBL33109;Pentyl 2-hydroxypropanoate #;DTXSID70858752;PENTYL 2-HYDROXYPROPIONATE;EINECS 228-974-4;NSC406253;AKOS006273939;NSC 406253;AI3-00588;FT-0622376;Q27284472

Chemical Property of Amyl lactate

Chemical Property:

• Vapor Pressure: 0.0624mmHg at 25°C
• Refractive Index: 1.436
• Boiling Point: 204.6 °C at 760 mmHg
• Flash Point: 79.2 °C
• PSA: 46.53000
• Density: 0.989 g/cm³
• LogP: 1.10060
• Water Solubility.: 10g/L(25 oC)
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 160.109944368
• Heavy Atom Count: 11
• Complexity: 112

Purity/Quality:

99%, ^*data from raw suppliers

AMYL LACTATE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCOC(=O)C(C)O

Technology Process of Amyl lactate

There total 10 articles about Amyl lactate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

C15H21NO4 → propanoic acid, 2-hydroxy-, pentyl ester (6382-06-5,171056-23-8)

Guidance literature:

With methanol; copper (I) acetate; In chloroform; at 20 ℃; for 18h;

DOI:10.1016/S0040-4039(99)00332-9

Reference yield: 72.0%

Pyridine-2-carboxylic acid (S)-1-pentyloxycarbonyl-ethyl ester → propanoic acid, 2-hydroxy-, pentyl ester (6382-06-5,171056-23-8)

Guidance literature:

With methanol; copper (I) acetate; In chloroform; at 20 ℃; for 6h;

DOI:10.1016/S0040-4039(99)00332-9

Reference yield:

pentan-1-ol (71-41-0) + 2-oxopropanal (78-98-8) → propanoic acid, 2-hydroxy-, pentyl ester (6382-06-5,171056-23-8)

Guidance literature:

With titanium-silicon molecular sieve TS-1; tin-silicon molecular sieve Sn-Beta; at 60 ℃; for 7h;

upstream raw materials:

methyl lactate

pentan-1-ol

sodium lactate

calcium lactate

Refernces

• 1、 -. "Method for preparing lactate". Paragraph 0090-0091. . Retrieved 2020/06/30.
• 2、 Zhang, Jie,Yang, Changchun,Tang, Ying,Xu, Lianghong,Wang, Xiaoting. "Development of lactic ester as bifunctional additive of methanol-gasoline". . p. 4827 - 4829. Retrieved 2014/12/10.