ChemicalBook > CAS DataBase List > 2-Methyl-2-butanol

2-Methyl-2-butanol

Product Name
2-Methyl-2-butanol
CAS No.
75-85-4
Chemical Name
2-Methyl-2-butanol
Synonyms
TERT-AMYL ALCOHOL;T-AMYL ALCOHOL;2-METHYLBUTAN-2-OL;t-amyl;TERT-PENTANOL;AMYLENE HYDRATE;2-methyl-2-butano;TERT-PENTYL ALCOHOL;Tert-AmylAlcohol,99%;tert-Isoamyl alcohol
CBNumber
CB7854246
Molecular Formula
C5H12O
Formula Weight
88.15
MOL File
75-85-4.mol
More
Less

2-Methyl-2-butanol Property

Melting point:
-12 °C
Boiling point:
102 °C(lit.)
Density 
0.805 g/mL at 25 °C(lit.)
vapor density 
3 (vs air)
vapor pressure 
15.5 hPa (20 °C)
refractive index 
n20/D 1.405(lit.)
Flash point:
20 °C
storage temp. 
Store at +5°C to +30°C.
solubility 
Miscible with alcohol, ether, benzene, chloroform, glycerol, oils and acetone.
form 
Liquid
pka
15.38±0.29(Predicted)
color 
Clear colorless
PH
6.0 (118g/l, H2O, 20℃)neutral
Odor
pungent
Odor Threshold
0.088ppm
explosive limit
1.3-9.6%(V)
Water Solubility 
120 g/L (20 ºC)
Merck 
14,7140
BRN 
1361351
Dielectric constant
11.7(20℃)
Stability:
Light sensitive. Highly flammable. Incompatible with strong oxidizing agents.
LogP
0.890
CAS DataBase Reference
75-85-4(CAS DataBase Reference)
NIST Chemistry Reference
2-Butanol, 2-methyl-(75-85-4)
EPA Substance Registry System
2-Methyl-2-butanol (75-85-4)
More
Less

Safety

Hazard Codes 
F,Xn
Risk Statements 
11-20-37/38-41-21
Safety Statements 
46-39-36/37-26
RIDADR 
UN 1105 3/PG 2
OEB
A
OEL
TWA: 100.0 ppm; 360.0 mg/m3, STEL: 125.0 ppm; 450.0 mg/m3
WGK Germany 
1
RTECS 
SC0175000
Autoignition Temperature
819 °F
TSCA 
Yes
HazardClass 
3
PackingGroup 
II
HS Code 
29051500
Hazardous Substances Data
75-85-4(Hazardous Substances Data)
Toxicity
LD50 orally in rats: 1.0 g/kg (Schaffarzick, Brown)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H315Causes skin irritation

H318Causes serious eye damage

H335May cause respiratory irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.06193
Product name
tert-Amyl alcohol
Purity
EMPLURA?
Packaging
1L
Price
$165
Updated
2024/03/01
Sigma-Aldrich
Product number
19954
Product name
2-Methyl-2-butanol
Purity
analytical standard
Packaging
1mL
Price
$31.4
Updated
2024/03/01
Sigma-Aldrich
Product number
19954
Product name
2-Methyl-2-butanol
Purity
analytical standard
Packaging
5ml
Price
$118
Updated
2024/03/01
Sigma-Aldrich
Product number
152463
Product name
2-Methyl-2-butanol
Purity
ReagentPlus , 99%
Packaging
1l
Price
$139
Updated
2024/03/01
Sigma-Aldrich
Product number
152463
Product name
2-Methyl-2-butanol
Purity
ReagentPlus , 99%
Packaging
2.5l
Price
$267
Updated
2024/03/01
More
Less

2-Methyl-2-butanol Chemical Properties,Usage,Production

Chemical Properties

colourless liquid with a camphor-like odour

Chemical Properties

Amyl alcohol is produced during the fermentation of grains, potatoes, and beets. It is also produced during the acid hydrolysis of petroleum fraction. Amyl alcohol is widely used in industry. For example, in the manufacturing of lacquers, paints, varnishes, perfumes, pharmaceuticals, plastics, rubber, explosives, hydraulic fl uids, for the extraction of fats, is also used in the petroleum refi nery industries

Chemical Properties

Amyl alcohols (pentanols) have eight isomers. All are flammable, colorless liquids, except the isomer 2,2- dimethyl-1-propanol, which is a crystalline solid.

Chemical Properties

tert-Amyl alcohol is a volatile liquid.2-Methyl-2-butanol has a sour odor, a threshold value of 8.2 mg/m3 (2.3 ppm), an absolute perception limit of 0.04 ppm, and a 100% recognition level of 0.23 ppm .

Uses

2-Methyl-2-butanol is used as a solvent in flavors, pharmaceuticals, corrosion inhibitors, resins, gums, coating materials and in organic synthesis. It acts as a frothing agent (ore flotation), surfactant (petroleum recovery) and stabilizing agent. Further, it is used in processing aids.

Uses

2-Methyl-2-butanol has been used in evaluating esterification rate of natural antioxidants like cinnamic acid and ascorbic acid using HPLC.

Uses

Pharmaceutic aid (solvent).

Definition

ChEBI: A tertiary alcohol that is propan-1-ol in which both of the hydrogens at position 1 have been replaced by methyl groups.

Production Methods

tert-Amyl alcohol is prepared by hydrating 2-methyl-2- butenes. It can also be prepared by reducing pivalic acid.

General Description

A clear, colorless liquid with an odor of camphor. Flash point 70°F. Density 0.81 g / cm3. Slightly soluble in water.

Air & Water Reactions

Highly flammable. Slightly soluble in water.

Reactivity Profile

2-Methyl-2-butanol attacks plastics [Handling Chemicals Safely 1980. p. 236]. Reacts violently with acetyl bromide [Merck 11th ed. 1989]. Mixtures of alcohols with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. Example: an explosion will occur if dimethylbenzylcarbinol is added to 90% hydrogen peroxide then acidified with concentrated sulfuric acid. Mixtures of ethyl alcohol with concentrated hydrogen peroxide form powerful explosives. Mixtures of hydrogen peroxide and 1-phenyl-2-methyl propyl alcohol tend to explode if acidified with 70% sulfuric acid [Chem. Eng. News 45(43):73 1967; J, Org. Chem. 28:1893 1963]. Alkyl hypochlorites are violently explosive. They are readily obtained by reacting hypochlorous acid and alcohols either in aqueous solution or mixed aqueous-carbon tetrachloride solutions. Chlorine plus alcohols would similarly yield alkyl hypochlorites. They decompose in the cold and explode on exposure to sunlight or heat. Tertiary hypochlorites are less unstable than secondary or primary hypochlorites [NFPA 491 M, 1991]. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence [Wischmeyer 1969].

Hazard

Flammable, dangerous fire risk.

Health Hazard

Inhalation of the vapors of amyl alcohol causes tearing, pain, redness, swelling, irritation of the mucous membrane of the eyes, nose, throat, and upper respiratory tract and of thskin. Acute and long-term exposure to amyl alcohol causes nausea, vomiting, headache, vertigo, and muscular weakness. Vomiting may cause aspiration into the lungs, resulting in chemical pneumonia. After a prolonged period of exposure to amyl alcohol, workers develop dizziness, double vision, shortness of breath, delirium, and related narcotic effects. In severe cases, inhalation leads to pulmonary edema, kidney injury, effects on the heart and becomes fatal. Occupational workers with pre-existing skin disorders, eye problems, or impaired liver, kidney, or respiratory function, may be more susceptible to the effects of amyl alcohol.

Health Hazard

Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control may cause pollution.

Fire Hazard

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Safety Profile

Moderately toxic to humans by an unspecified route. Moderately toxic experimentally by ingestion, intraperitoneal, subcutaneous, and rectal routes. Narcotic in high concentration. Flammable liquid when exposed to heat, flame, or oxiduing materials. Moderately explosive in the form of vapor when exposed to heat or flame. A hypnotic agent. When heated to decomposition it emits acrid smoke and irritating fumes.

Potential Exposure

(n-isomer); Suspected reprotoxic hazard, Primary irritant (w/o allergic reaction), (iso-, primary): Possible risk of forming tumors, Primary irritant (w/o allergic reaction), (sec-, active primary-, and other isomers) Primary irritant (w/o allergic reaction). Used as a solvent in organic synthesis and synthetic flavoring, pharmaceuticals, corrosion inhibitors; making plastics and other chemicals; as a flotation agent. The (n-isomer) is used in preparation of oil additives, plasticizers, synthetic lubricants, and as a solvent.

Shipping

UN2811 Pentanols, Hazard Class: 3; Labels: 3- Flammable liquid. UN1987 Alcohols, n.o.s., Hazard Class: 3; Labels: 3-Flammable liquid.

Purification Methods

Reflux it with K2CO3, CaH2, CaO or sodium, then fractionally distil. The near-dry alcohol is further dried by refluxing with Mg activated with iodine, as described for ethanol. Further purification is possible using fractional crystallisation and zone refining at <-10o or preparative gas chromatography. [Beilstein 1 IV 1668.]

Incompatibilities

Forms an explosive mixture with air. Contact with strong oxidizers and hydrogen trisulfide may cause fire and explosions. Incompatible with strong acids. Violent reaction with alkaline earth metals forming hydrogen, a flammable gas.

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

Precautions

During handling and use of amyl alcohol, persons with pre-existing skin disorders, eye problems, or impaired liver, kidney, or respiratory function, should be careful since these workers/persons are more susceptible to the effects of amyl alcohol

More
Less

2-Methyl-2-butanol Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
Tedia Company
Tel
--
Fax
--
Email
sales@tedia.com
Country
United States
ProdList
52
Advantage
58
Veckridge Chemical
Tel
--
Fax
--
Email
rv@veckridge.com
Country
United States
ProdList
87
Advantage
58
MilliporeSigma (Sigma-Aldrich Corp.)
Tel
--
Fax
--
Email
@sial.com
Country
United States
ProdList
5414
Advantage
58
Brenntag North America, Inc.
Tel
--
Fax
--
Email
bnereadingcs@brenntag.com
Country
United States
ProdList
211
Advantage
58
Pan Asian Chemicals Inc.
Tel
--
Fax
--
Email
info@panasianchem.com
Country
United States
ProdList
109
Advantage
58
Lab Express International
Tel
--
Fax
--
Email
@labexpress.com
Country
United States
ProdList
307
Advantage
58
MP Biomedicals, LLC. (Division of Valiant FC Co., Ltd.)
Tel
--
Fax
--
Email
serv@mpbio.com
Country
United States
ProdList
1854
Advantage
58
Redox Scientific
Tel
--
Fax
--
Email
info@redoxsci.com
Country
United States
ProdList
2380
Advantage
58
Beantown Chemical Corporation
Tel
--
Fax
--
Country
United States
ProdList
396
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
Parchem Fine & Specialty Chemicals
Tel
--
Fax
--
Email
info@parchem.com
Country
United States
ProdList
1031
Advantage
58
BASF SE
Tel
--
Fax
--
Email
jennifer.moore-braun@basf.com
Country
United States
ProdList
285
Advantage
58
TCI America, Inc. (part of Tokyo Chemical Industry)
Tel
--
Fax
--
Email
Angelina.Crew@tcichemicals.com
Country
United States
ProdList
2053
Advantage
58
Penta Manufacturing Company (a division of Penta International Corporation)
Tel
--
Fax
--
Email
@pentamfg.com
Country
United States
ProdList
901
Advantage
58
Wego Chemical Group
Tel
--
Fax
--
Email
sales@wegochem.com
Country
United States
ProdList
443
Advantage
58
Huntsman Corporation
Tel
--
Fax
--
Email
hpporders@huntsman.com
Country
United States
ProdList
28
Advantage
58
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
Century Multech Inc.
Tel
--
Fax
--
Email
rylchu@aol.com
Country
United States
ProdList
53
Advantage
30
Chem Service, Inc
Tel
--
Fax
--
Country
United States
ProdList
240
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
Penta International Corporation
Tel
--
Fax
--
Email
lisaa@pentamfg.com
Country
United States
ProdList
5042
Advantage
58
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Chemstock Inc.
Tel
--
Fax
--
Email
mail@chemstock.com
Country
United States
ProdList
575
Advantage
34
Santa Cruz Biotechnology, Inc.
Tel
--
Fax
--
Email
scbt@scbt.com
Country
United States
ProdList
3597
Advantage
60
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
ChemService Inc.
Tel
--
Fax
--
Country
United States
ProdList
6379
Advantage
68
ChemSampCo, Inc.
Tel
--
Fax
--
Email
sales@chemsampco.com
Country
United States
ProdList
3585
Advantage
60
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
Narchem Corporation
Tel
--
Fax
--
Email
sales@narchem.com
Country
United States
ProdList
2813
Advantage
60
BASF Corporation
Tel
--
Fax
--
Country
United States
ProdList
573
Advantage
86
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
Penta Manufacturing Company
Tel
--
Fax
--
Email
sales@pentamfg.com
Country
United States
ProdList
5076
Advantage
65
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
Naugra Export
Tel
--
Fax
--
Country
United States
ProdList
1332
Advantage
47
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
City Chemical LLC
Tel
--
Fax
--
Email
sales@citychemical.com
Country
United States
ProdList
6708
Advantage
72
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
Leonid Chemicals Private Limited
Tel
--
Fax
--
Email
careers@leonidchemicals.com
Country
United States
ProdList
1700
Advantage
43
Loba Chemie Pvt. Ltd.
Tel
--
Fax
--
Country
United States
ProdList
1945
Advantage
71
ChromaDex
Tel
--
Fax
--
Email
sales@chromadex.com
Country
United States
ProdList
2501
Advantage
76
Crescent Chemical Co., Inc.
Tel
--
Fax
--
Email
sales@creschem.com
Country
United States
ProdList
4597
Advantage
68
MP Biomedicals, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6561
Advantage
81
EMD Chemicals Inc.
Tel
--
Fax
--
Email
emdinfo@emdchemicals.com
Country
United States
ProdList
1525
Advantage
77
More
Less

View Lastest Price from 2-Methyl-2-butanol manufacturers

Hebei Weibang Biotechnology Co., Ltd
Product
2-Methyl-2-butanol 75-85-4
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-22
Hebei Chuanghai Biotechnology Co,.LTD
Product
2-Methyl-2-butanol 75-85-4
Price
US $5.00-2.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10000kg
Release date
2024-08-23
Hebei Mojin Biotechnology Co., Ltd
Product
2-Methyl-2-butanol 75-85-4
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
1000tons
Release date
2023-08-15

75-85-4, 2-Methyl-2-butanolRelated Search:


  • 2-methyl-2-butano
  • 2-methyl-2-butanol (tert-amyl alcohol)
  • 2-methylbutanol-2
  • 3-Methylbutan-3-ol
  • 3-Methyl-butanol-(3)
  • Amylenhydrate
  • C2H5C(CH3)2OH
  • Methyl-2 butanol-2
  • Methyl-3 butanol-3
  • AMYL ALCOHOL, TERT-
  • AMYLENE HYDRATE
  • 2-METHYL-2-BUTANOL REAGENTPLUSTM >=99%
  • TERT-AMYL ALCOHOL REAGENTPLUS(TM) 99%
  • 2-METHYL-2-BUTANOL, REAGENTPLUS, >=99%
  • TERT-AMYL ALCOHOL, REAGENTPLUS, 99%
  • Tert-AmylAlcoholGr
  • Tert-AmylAlcoholForSynthesis
  • Tert-AmylAlcohol,99%
  • TERT-AMYL ALCOHOL, REAG.
  • 2-Methyl-2-butanol, 99+%
  • TERT-AMYLALCOHOL,REAGENT
  • TERTIARYPENTYLALCOHOL
  • tert.Amylalkohol
  • 2-methylbutan-2-ol tert-pentanol
  • tert-Isoamyl alcohol
  • t-pentylalcohol
  • ETHYLDIMETHYLCARBINOL
  • DIMETHYLETHYLCARBINOL
  • 2-METHYL-2-BUTANOL
  • 2-METHYLBUTAN-2-OL
  • TERT-PENTYL ALCOHOL
  • TERT-PENTANOL
  • TERT-AMYL ALCOHOL
  • T-AMYL ALCOHOL
  • 1,1-Dimethyl-1-propanol
  • 2-butanol,2-methyl-
  • 2-Methyl butanol-2
  • tert-Amyl alcohol, tert-Pentyl alcohol
  • Ethyldimethylcarbinol 2-Methyl-2-butanol tert-Pentanol
  • 2-Methyl-2-butanol, 99+%, extra pure
  • TERT-AMYL ALCOHOL EMPLURA
  • 2-Methyl-2-butanol,tert-Amyl alcohol, tert-Pentyl alcohol
  • 2-Methyl-2-butanol, extra pure, 99+%
  • 2-Methyl-2-butanol, pure, 99%
  • 2-Methyl-2-butanol, 99%, pure
  • 2-Methyl-2-butanol, 99% 1LT
  • 2-Methyl-2-butanol, 99% 2.5LT
  • 2-Methyl-2-butanol, 99+% 5ML
  • 2-Methyl-2-butanol anhydrous, >=99%
  • 2-Methyl-2-butanol ReagentPlus(R), >=99%
  • 2-Methyl-2-butanol ReagentPlus(R), 99%
  • 2-Methyl-2-butanol 〔t-Amyl Alcohol〕
  • t-Amyl Alchohol
  • t-amyl
  • Tertiaryamylalcohol
  • tert-AmylAlcoholSolutionSecondSource,2,000mg/L,1ml
  • tert-AmylAlcoholSolution,200mg/L,1ml
  • tert-AmylAlcohol&gt