(3-Methylbutoxy)acetic acid

Base Information

Chemical Name:(3-Methylbutoxy)acetic acid
CAS No.:68298-29-3
Molecular Formula:C7H14O3
Molecular Weight:146.186
Hs Code.:2918990090
European Community (EC) Number:269-553-5
DSSTox Substance ID:DTXSID5071383
Nikkaji Number:J289.136K
Wikidata:Q81998996
Mol file:68298-29-3.mol

Synonyms:2-(3-methylbutoxy)acetic acid;MBAA cpd

Suppliers and Price of (3-Methylbutoxy)acetic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
2-(3-METHYLBUTOXY)ACETIC ACID 95.00%
5G
$ 1548.26

American Custom Chemicals Corporation
2-(3-METHYLBUTOXY)ACETIC ACID 95.00%
2.5G
$ 1227.82

American Custom Chemicals Corporation
2-(3-METHYLBUTOXY)ACETIC ACID 95.00%
1G
$ 852.55

AK Scientific
(3-Methylbutoxy)aceticacid
100mg
$ 264.00

Total 7 raw suppliers

Chemical Property of (3-Methylbutoxy)acetic acid

Chemical Property:

Vapor Pressure:0.0082mmHg at 25°C
Boiling Point:247.6°Cat760mmHg
Flash Point:96.8°C
PSA：46.53000
Density:1.005g/cm³
LogP:1.13370
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:146.094294304
Heavy Atom Count:10
Complexity:99

Purity/Quality:

99% ^*data from raw suppliers

2-(3-METHYLBUTOXY)ACETIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CCOCC(=O)O

Technology Process of (3-Methylbutoxy)acetic acid

There total 4 articles about (3-Methylbutoxy)acetic acid 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: 97.7%

: 623-73-4
diazoacetic acid ethyl ester

: 123-51-3
i-Amyl alcohol

: 68298-29-3
isoamyloxyacetic acid

Guidance literature:: With dirhodium tetraacetate; In 1,2-dichloro-ethane; at 85 ℃; for 3.5h; Inert atmosphere;

Reference yield: 95.0%

: Allyl isoamyl glycolate

: 68298-29-3
isoamyloxyacetic acid

Guidance literature:: Allyl isoamyl glycolate; With sodium hydroxide; water; In methanol; for 1h;

With hydrogenchloride; In methanol; water; pH=3;