3-PHENYL-1-BUTANOL

CAS No.：2722-36-3

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This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
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3-PHENYL-1-BUTANOL Basic information

Product Name:	3-PHENYL-1-BUTANOL
Synonyms:	RARECHEM AL BD 0683;(±)-3-phenyl-butan-1-ol;Benzenepropanol, gamma-methyl-;gamma-methyl-benzenepropano;3-PHENYL-1-BUTANOL;3-Phenylbutyl alcohol.;3-PHENYL-1-BUTANOL 99%;3-Phenyl-1-butanol,99%
CAS:	2722-36-3
MF:	C10H14O
MW:	150.22
EINECS:	220-335-8
Product Categories:	Alcohols;C9 to C30;Oxygen Compounds
Mol File:	2722-36-3.mol

3-PHENYL-1-BUTANOL Chemical Properties

Boiling point	138-140 °C33 mm Hg(lit.)
density	0.972 g/mL at 25 °C(lit.)
refractive index	n20/D 1.52(lit.)
Fp	>230 °F
storage temp.	Refrigerator
solubility	Acetonitrile (Slightly), Chloroform (Slightly)
pka	15.04±0.10(Predicted)
form	Oil
color	Colourless
CAS DataBase Reference	2722-36-3

Safety Information

Safety Statements	24/25
WGK Germany	3
HS Code	29062900

MSDS Information

Provider	Language
SigmaAldrich	English
ACROS	English

3-PHENYL-1-BUTANOL Usage And Synthesis

Chemical Properties	CLEAR COLOURLESS LIQUID
Uses	3-Phenyl-1-butanol is a reactant with primary alcohol functional group which is oxidized to aldehyde using the nanoparticle-ferrite-palladium catalyst.
General Description	3-Phenyl-1-butanol undergoes biotransformation to aldehydes by oxidation in the presence of Gluconobacteroxydans DSM 2343. It undergoes enantioselective transesterification reaction with vinyl acetate catalyzed by lipase isolated from Pseudomonas cepacia.

3-PHENYL-1-BUTANOL Preparation Products And Raw materials

Raw materials

Cyclohexanamine, N-(2E)-2-buten-1-ylidene-, [N(E)]--->3-Phenyl-but-2-en-1-ol-->4-methyl-4-phenyl-1,3-dioxane-->2-(Phenyl)succinic acid dimethyl ester-->but-3-en-2-ylbenzene-->2-methyl-2-phenyloxetane-->diethyl 2-phenylbutanedioate-->(R)-2-phenylbutane-1,4-diol-->3-PHENYLBUTYRALDEHYDE-->3-PHENYL-CYCLOBUTAN-1-ONE-->carbon monoxide-->2-Phenyl-1-propene-->Phenyllithium

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