ChemicalBook >> CAS DataBase List >>Monomethyl adipate

Monomethyl adipate

CAS No.
627-91-8
Chemical Name:
Monomethyl adipate
Synonyms
6-Methoxy-6-oxohexanoic acid;Adipic acid monometh;ADIPIC ACID MONOMETHYL ESTER;NSC55113;NSC 55113;NSC-55113;METHYL ADIPATE;Methyladipinate;Methyl hemiadipate;MONO-METHYL ADIPATE
CBNumber:
CB9683693
Molecular Formula:
C7H12O4
Molecular Weight:
160.17
MDL Number:
MFCD00004418
MOL File:
627-91-8.mol
MSDS File:
SDS
Last updated:2026-01-13 11:27:10
Product description Number Pack Size Price
mono-Methyl adipate 99% A26403 5g $60.7
mono-Methyl adipate 99% A26403 25g $104
Monomethyl Adipate >97.0%(GC)(T) A1738 25g $59
Monomethyl Adipate >97.0%(GC)(T) A1738 100g $181
mono-Methyl adipate M564800 25g $220
More product size

Monomethyl adipate Properties

Melting point 7-9 °C (lit.)
Boiling point 162 °C/10 mmHg (lit.)
Density 1.081 g/mL at 25 °C (lit.)
vapor pressure 1.48Pa at 25℃
refractive index n20/D 1.441(lit.)
Flash point >230 °F
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Sparingly), Methanol (Slightly)
pka 4.69±0.10(Predicted)
form Liquid
color Clear colorless
Water Solubility Not miscible or difficult to mix with water.
BRN 1766411
InChI 1S/C7H12O4/c1-11-7(10)5-3-2-4-6(8)9/h2-5H2,1H3,(H,8,9)
InChIKey UOBSVARXACCLLH-UHFFFAOYSA-N
SMILES COC(=O)CCCCC(O)=O
LogP 0.500 (est)
CAS DataBase Reference 627-91-8(CAS DataBase Reference)
FDA UNII 62S39VHD01
NIST Chemistry Reference Hexanedioic acid, monomethyl ester(627-91-8)
EPA Substance Registry System Monomethyl adipate (627-91-8)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
PPE Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  24/25-36-26
WGK Germany  3
TSCA  TSCA listed
HS Code  29171290
Storage Class 10 - Combustible liquids
NFPA 704
0
2 0

Monomethyl adipate price More Price(24)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich A26403 mono-Methyl adipate 99% 627-91-8 5g $60.7 2025-07-31 Buy
Sigma-Aldrich A26403 mono-Methyl adipate 99% 627-91-8 25g $104 2025-07-31 Buy
TCI Chemical A1738 Monomethyl Adipate >97.0%(GC)(T) 627-91-8 25g $59 2025-07-31 Buy
TCI Chemical A1738 Monomethyl Adipate >97.0%(GC)(T) 627-91-8 100g $181 2025-07-31 Buy
TRC M564800 mono-Methyl adipate 627-91-8 25g $220 2021-12-16 Buy
Product number Packaging Price Buy
A26403 5g $60.7 Buy
A26403 25g $104 Buy
A1738 25g $59 Buy
A1738 100g $181 Buy
M564800 25g $220 Buy

Monomethyl adipate Chemical Properties,Uses,Production

Chemical Properties

clear colorless liquid

Uses

Methyl hydrogen adipate is a useful synthetic intermediate. It can be used to prepare 1,3,4-thiadiazole hydroxamic acid derivatives as novel histone deacetylase inhibitors which show potential antitumor activities. It can be also used to synthesize mannose-linked biphenylylacetic acid derivatives as novel inhibitors of selectin-mediated cell adhesion.

Definition

ChEBI: Monomethyl adipate is a dicarboxylic acid monoester that is the monomethyl ester of adipic acid. It has a role as a metabolite and a plasticiser.

Synthesis

According to the general procedure described above, a has been synthesized from adipic acid (730mg, 5 mmol) and methanol (10 ml). Yield: 80%.
The synthetic method of Monomethyl adipate mainly contains following three kinds:
The one, under alkaline condition or issue the first portion hydrolysis reaction in the catalysis of bioactive enzyme (pork liver lipase etc.) and obtain Monomethyl adipate (such as document Blaise; Koehler; Bulletin de la Societe Chimique deFrance; Vol. (4) 7; (1910); P.219).
The 2nd, by hexanodioic acid or adipic anhydride and ethanol, as catalyzer, the control reaction conditions carries out esterification and obtains Monomethyl adipate (such as document Chem.Zentralbl. with acid; Vol.97; (1926; P.126));
The 3rd, by the people such as Swann nineteen forty-three with hexanodioic acid, diethylene adipate and ethanol with the condition of acid as catalyst under control reaction conditions obtain monomethyl adipate(document such as Swann; Oehler; Buswell; Org.synth.Coll.Vol.11; (1943); P.227).
Synthetic method of monomethyl adipate
http://www.orgsyn.org/demo.aspx?prep=CV2P0264

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View Lastest Price from Monomethyl adipate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Monomethyl adipate pictures 2026-01-30 Monomethyl adipate
627-91-8
US $0.00-0.00 / KG 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
Monomethyl adipate pictures 2025-05-26 Monomethyl adipate
627-91-8
US $100.00-50.00 / KG 1KG 99% 10000kg Hebei Chuanghai Biotechnology Co,.LTD
Monomethyl adipate pictures 2025-04-15 Monomethyl adipate
627-91-8
US $50.00 / kg 1kg 99 5000 Hebei Zhuanglai Chemical Trading Co.,Ltd
Hexanedioic acid hydrogen 1-methyl Adipic acid monometh MonoMethyl adipate, 98% 5GR Adipic acid 1-methyl ester Adipic acid hydrogen 1-methyl Adipic acid hydrogen 1-methyl ester Hexanedioic acid 1-methyl Adipic Acid Monomethyl Ester Methyl Hydrogen Adipate Monomethyl Hexanedioate Hexanedioic Acid Monomethyl Ester Hexanedioic acid,1-Methyl ester Mono-Methyl adipate 99% 6-Methoxy-6-oxohexanoic acid Methyl 5-carboxypentanoate Methyl hemiadipate ADIPIC ACID MONOMETHYL ESTER METHYL ADIPATE METHYL HYDROGEN HEXANE-1,6-DIOATE METHYL HYDROGEN ADIPATE hexanedioic acid monomethyl ester MONOMETHYL HEXANE-1,6-DIOATE MONO-METHYL ADIPATE MonomethylAdipate98% Methylhydrogeneadipate Adipic acid methyl ester Dihexanoic acid methyl ester HEXANEDIOICACID,MONOMETHYLE Methyladipinate 5-Carbomethoxypentanoic acid Monomethyl 1,6-hexanedioate Adipic acid 1-methyl Adipic acid monomethyl ester, mono-Methyl adipate, Monomethyl adipate Adipic acid monomethyl ester, Monomethyl adipate Monomethyl Adipate > Monomethyl Hexanedioate 627-91-8 (MONOMETHYL ADIPATE) NSC 55113 NSC55113 NSC-55113 Monomethyl adipate in methanol 6-Methoxy-6-oxo-hexanoic acid 98% 627-91-8 4089-07-2 HO2CCH24CO2CH3 CH3O2CCH24CO2H C7H11O4 Carbonyl Compounds C6 to C7 Building Blocks Organic Building Blocks Esters CARBOXYLIC ACID Building Blocks C6 to C7 Carbonyl Compounds Senior lubricating oil Chemical Synthesis Esters Organic Building Blocks 1