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1-Pentanol, 5-butoxy-, also known as 5-butoxypentan-1-ol or butyl glyceryl ether, is a colorless liquid with a molecular formula of C9H20O2. It is an ether derivative of pentanol, where a butoxy group (C4H9O) is attached to the primary hydroxyl group of pentanol. This organic compound is used as a solvent, emulsifier, and intermediate in the synthesis of various chemicals, including surfactants and pharmaceuticals. It is characterized by its low toxicity, high boiling point (around 200°C), and solubility in water. Due to its versatile properties, 1-pentanol, 5-butoxy- plays a significant role in various industrial applications, particularly in the production of consumer goods and specialty chemicals.

4541-05-3

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4541-05-3 Usage

Physical state

Colorless liquid

Odor

Characteristic odor

Industrial applications

Solvent, manufacturing of perfumes and flavorings

Usage

Intermediate in the synthesis of other organic compounds

Solubility

Ability to dissolve a wide range of substances

Toxicity

Relatively low

Carcinogenicity

Not classified as a carcinogen

Mutagenicity

Not classified as a mutagen

Reproductive toxicity

Not classified as a reproductive toxicant

Health hazards

May cause irritation to skin, eyes, and respiratory system

Safety precautions

Handle with care in a well-ventilated area.

Check Digit Verification of cas no

The CAS Registry Mumber 4541-05-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,4 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4541-05:
(6*4)+(5*5)+(4*4)+(3*1)+(2*0)+(1*5)=73
73 % 10 = 3
So 4541-05-3 is a valid CAS Registry Number.

4541-05-3Upstream product

4541-05-3Downstream Products

4541-05-3Relevant academic research and scientific papers

Opening of Cyclic Acetals by Trichloro-, Dichloro- and Tribromo-borane

Bonner, Trevor G.,Lewis, David,Rutter, Keith

, p. 1807 - 1810 (2007/10/02)

The rate-determining step in the ring opening of cyclic acetals by trichloroborane to yield α-chloro-ethers is shown to be consistent with the formation of an oxocarbenium ion.Subsequent reduction provides a general route for the conversion of a diol into a hydroxy-ether.Tribromoborane is a more powerful and dichloroborane a less powerful reagent than trichloroborane.

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