methoxymethyl butanol

butan-1-ol, 3-methoxy-3-methyl-

CAS: 56539-66-3 C6 H14 O2 MW: 118.17598000

Identification

Namemethoxymethyl butanol
CAS Number56539-66-3
EINECS260-252-4
FDA UNII366754K2K1
Molecular FormulaC6 H14 O2
Molecular Weight118.17598000
MDL NumberMFCD00044771
Nikkaji NumberJ38.165I
Beilstein1732882

Regulatory

Physical Properties

Appearance colorless clar liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.92700 to 0.93000 @ 20.00 °C.
Pounds per Gallon - (est). 7.723 to 7.748
Refractive Index 1.42500 to 1.42800 @ 20.00 °C.
Boiling Point 163.00 to 165.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.675000 mmHg @ 25.00 °C. (est)
Flash Point 160.00 °F. TCC ( 71.11 °C. )
logP (o/w) 0.481 (est)
Soluble in alcohol
Insoluble in water

Cosmetic Information

CosIngcosmetic data
Cosmetic Usessolvents

Organoleptic Properties

Odor Description Practically odourless

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorysolvents
Recommendation for methoxymethyl butanol usage levels up tonot for fragrance use.
Recommendation for methoxymethyl butanol flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

butan-1-ol, 3-methoxy-3-methyl- 1- butanol, 3-methoxy-3-methyl- methoxy-3 3-methyl butanol 3- methoxy-3-methyl butanol 3- methoxy-3-methyl-1-butanol 3- methoxy-3-methyl-butan-1-ol 3- methoxy-3-methylbutan-1-ol 3- methoxy-3-methylbutanol 3- methyl-3-methoxybutanol US Patents: 5,585,343 - Low VOC perfume formulations PubMed: Kinetics and products of the reaction of OH radicals with 3-methoxy-3-methyl-1-butanol. PubMed: Identification of potent odourants in wine and brewed coffee using gas chromatography-olfactometry and comprehensive two-dimensional gas chromatography. PubMed: The phosphodiesterase 3 inhibitor cilostamide enhances inotropic responses to glucagon but not to dobutamine in rat ventricular myocardium.