{"id":6318,"date":"2023-03-08T07:46:47","date_gmt":"2023-03-08T07:46:47","guid":{"rendered":"https:\/\/masterchem.lv\/?post_type=product&#038;p=6318"},"modified":"2025-06-17T12:58:09","modified_gmt":"2025-06-17T12:58:09","slug":"n-propyl-alcohol-cas-71-23-8","status":"publish","type":"product","link":"https:\/\/masterchem.lv\/en\/product\/n-propyl-alcohol-cas-71-23-8\/","title":{"rendered":"N-propyl alcohol (CAS 71-23-8)"},"content":{"rendered":"<p style=\"text-align: justify;\">1-Propanol shows the normal reactions of a\u00a0<a title=\"Primary alcohol\" href=\"https:\/\/en.wikipedia.org\/wiki\/Primary_alcohol\">primary alcohol<\/a>. Thus it can be converted to\u00a0<a title=\"Haloalkane\" href=\"https:\/\/en.wikipedia.org\/wiki\/Haloalkane\">alkyl halides<\/a>; for example red\u00a0<a title=\"Phosphorus\" href=\"https:\/\/en.wikipedia.org\/wiki\/Phosphorus\">phosphorus<\/a>\u00a0and\u00a0<a title=\"Iodine\" href=\"https:\/\/en.wikipedia.org\/wiki\/Iodine\">iodine<\/a>\u00a0produce\u00a0<a class=\"mw-redirect\" title=\"N-propyl iodide\" href=\"https:\/\/en.wikipedia.org\/wiki\/N-propyl_iodide\">n-propyl iodide<\/a>\u00a0in 80% yield, while\u00a0<a title=\"Phosphorus trichloride\" href=\"https:\/\/en.wikipedia.org\/wiki\/Phosphorus_trichloride\">PCl<sub>3<\/sub><\/a>\u00a0with catalytic\u00a0<a title=\"Zinc chloride\" href=\"https:\/\/en.wikipedia.org\/wiki\/Zinc_chloride\">ZnCl<sub>2<\/sub><\/a>\u00a0gives\u00a0<a class=\"mw-redirect\" title=\"N-propyl chloride\" href=\"https:\/\/en.wikipedia.org\/wiki\/N-propyl_chloride\">n-propyl chloride<\/a>. Reaction with\u00a0<a title=\"Acetic acid\" href=\"https:\/\/en.wikipedia.org\/wiki\/Acetic_acid\">acetic acid<\/a>\u00a0in the presence of an\u00a0<a title=\"Sulfuric acid\" href=\"https:\/\/en.wikipedia.org\/wiki\/Sulfuric_acid\">H<sub>2<\/sub>SO<sub>4<\/sub><\/a>\u00a0catalyst under\u00a0<a class=\"mw-redirect\" title=\"Fischer esterification\" href=\"https:\/\/en.wikipedia.org\/wiki\/Fischer_esterification\">Fischer esterification<\/a>\u00a0conditions gives propyl acetate, while refluxing propanol overnight with formic acid alone can produce propyl formate in 65% yield. Oxidation of 1-propanol with\u00a0<a title=\"Sodium dichromate\" href=\"https:\/\/en.wikipedia.org\/wiki\/Sodium_dichromate\">Na<sub>2<\/sub>Cr<sub>2<\/sub>O<sub>7<\/sub><\/a>\u00a0and H<sub>2<\/sub>SO<sub>4<\/sub>\u00a0gives only a 36% yield of\u00a0<a title=\"Propionaldehyde\" href=\"https:\/\/en.wikipedia.org\/wiki\/Propionaldehyde\">propionaldehyde<\/a>, and therefore for this type of reaction higher yielding methods using\u00a0<a title=\"Pyridinium chlorochromate\" href=\"https:\/\/en.wikipedia.org\/wiki\/Pyridinium_chlorochromate\">PCC<\/a>\u00a0or the\u00a0<a title=\"Swern oxidation\" href=\"https:\/\/en.wikipedia.org\/wiki\/Swern_oxidation\">Swern oxidation<\/a>\u00a0are recommended. Oxidation with\u00a0<a title=\"Chromic acid\" href=\"https:\/\/en.wikipedia.org\/wiki\/Chromic_acid\">chromic acid<\/a>\u00a0yields\u00a0<a title=\"Propionic acid\" href=\"https:\/\/en.wikipedia.org\/wiki\/Propionic_acid\">propionic acid<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p style=\"text-align: justify;\"><b>Other names: 1-Propanol, n-Propanol, n-PrOH, Ethylcarbinol, 1-Hydroxypropane, Propionic alcohol, Propionyl alcohol, Propionylol, Propyl alcohol, Propylic alcohol, Propylol<\/b><\/p>\n<p style=\"text-align: justify;\">1-Propanol\u00a0is a\u00a0<a title=\"Primary alcohol\" href=\"https:\/\/en.wikipedia.org\/wiki\/Primary_alcohol\">primary alcohol<\/a>\u00a0with the formula CH<sub>3<\/sub>CH<sub>2<\/sub>CH<sub>2<\/sub>OH (sometimes\u00a0<a title=\"Skeletal formula\" href=\"https:\/\/en.wikipedia.org\/wiki\/Skeletal_formula#Pseudoelement_symbols\">represented<\/a>\u00a0as\u00a0PrOH\u00a0or\u00a0<i>n<\/i>-PrOH). This colorless liquid is also known as\u00a0propan-1-ol,\u00a01-propyl alcohol,\u00a0<i>n<\/i>-propyl alcohol, and\u00a0<i>n<\/i>-propanol. It is an\u00a0<a title=\"Isomer\" href=\"https:\/\/en.wikipedia.org\/wiki\/Isomer\">isomer<\/a>\u00a0of\u00a0<a class=\"mw-redirect\" title=\"2-propanol\" href=\"https:\/\/en.wikipedia.org\/wiki\/2-propanol\">2-propanol<\/a>\u00a0(propan-2-ol, isopropyl alcohol, isopropanol). It is formed naturally in small amounts during many fermentation processes and used as a solvent in the pharmaceutical industry mainly for resins and cellulose esters.<\/p>\n<p style=\"text-align: justify;\">\n<p>CAS: 71-23-8<\/p>\n","protected":false},"featured_media":6777,"template":"","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0},"product_brand":[],"product_cat":[167,101,86,110],"product_tag":[],"class_list":{"0":"post-6318","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-all-goods","7":"product_cat-pharmaceuticals","8":"product_cat-resins-plastics-polyurethanes","9":"product_cat-typography-chemicals","11":"first","12":"instock","13":"taxable","14":"shipping-taxable","15":"purchasable","16":"product-type-variable","17":"has-default-attributes"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>N-propyl alcohol (CAS 71-23-8) - \u0136\u012bmija r\u016bpniec\u012bbai &mdash; &Scaron;\u0137\u012bdin\u0101t\u0101ji un \u0137\u012bmisk\u0101s vielas &mdash; Masterchem.ee<\/title>\n<meta name=\"description\" content=\"1-Propanol is a primary alcohol with the formula CH3CH2CH2OH (sometimes represented as PrOH or n-PrOH). This colorless liquid is also known as propan-1-ol, 1-propyl alcohol, n-propyl alcohol, and n-propanol. CAS 71-23-8\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/masterchem.lv\/en\/product\/n-propyl-alcohol-cas-71-23-8\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"N-propyl alcohol (CAS 71-23-8) - \u0136\u012bmija r\u016bpniec\u012bbai &mdash; &Scaron;\u0137\u012bdin\u0101t\u0101ji un \u0137\u012bmisk\u0101s vielas &mdash; Masterchem.ee\" \/>\n<meta property=\"og:description\" content=\"1-Propanol is a primary alcohol with the formula CH3CH2CH2OH (sometimes represented as PrOH or n-PrOH). This colorless liquid is also known as propan-1-ol, 1-propyl alcohol, n-propyl alcohol, and n-propanol. 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This colorless liquid is also known as propan-1-ol, 1-propyl alcohol, n-propyl alcohol, and n-propanol. CAS 71-23-8","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/masterchem.lv\/en\/product\/n-propyl-alcohol-cas-71-23-8\/","og_locale":"en_US","og_type":"article","og_title":"N-propyl alcohol (CAS 71-23-8) - \u0136\u012bmija r\u016bpniec\u012bbai &mdash; &Scaron;\u0137\u012bdin\u0101t\u0101ji un \u0137\u012bmisk\u0101s vielas &mdash; Masterchem.ee","og_description":"1-Propanol is a primary alcohol with the formula CH3CH2CH2OH (sometimes represented as PrOH or n-PrOH). This colorless liquid is also known as propan-1-ol, 1-propyl alcohol, n-propyl alcohol, and n-propanol. 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