2-sec-Butylphenol

Product Name: 2-sec-Butylphenol
CAS No.: 89-72-5
Chemical Name: 2-sec-Butylphenol
Synonyms: OSBP;O-S-BUTYLPHENOL;2-sec.Butylfenol;O-SEC-BUTYLPHENOL;2-SEC-BUTYLPHENOL;2-(2-butyl)phenol;o-sec-butyl-pheno;2-sek.Butylphenol;0-sec-butylphenol;Phenol,o-sec-butyl-
CBNumber: CB4734578
Molecular Formula: C10H14O
Formula Weight: 150.22
MOL File: 89-72-5.mol

More

Less

2-sec-Butylphenol Property

Melting point:: 12 °C(lit.)
Boiling point:: 226-228 °C(lit.)
Density: 0.982 g/mL at 25 °C(lit.)
vapor pressure: 0.03 mm Hg ( 20 °C)
refractive index: n20/D 1.522(lit.)
Flash point:: 234 °F
pka: 10.36±0.35(Predicted)
form: Liquid
color: White to Light yellow
Water Solubility: Insoluble. <0.1 g/100 mL at 20 ºC
BRN: 1210026
Exposure limits: ACGIH: TWA 5 ppm (Skin)
NIOSH: TWA 5 ppm(30 mg/m3)
Stability:: Stable, but air sensitive. Incompatible with acid chlorides, acid anhydrides, bases, strong oxidizing agents, copper and its alloys, brass.
LogP: 3 at 20℃
CAS DataBase Reference: 89-72-5(CAS DataBase Reference)
NIST Chemistry Reference: Phenol, 2-(1-methylpropyl)-(89-72-5)
EPA Substance Registry System: o-sec-Butylphenol (89-72-5)

More

Less

Safety

Hazard Codes: C
Risk Statements: 20/21/22-34-22
Safety Statements: 26-27-28-36/37/39-45
RIDADR: UN 3145 8/PG 2
OEB: A
OEL: TWA: 5 ppm (30 mg/m3) [skin]
WGK Germany: 2
RTECS: SJ8920000
TSCA: Yes
HazardClass: 8
PackingGroup: III
HS Code: 29071910
Hazardous Substances Data: 89-72-5(Hazardous Substances Data)

More

Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H302Harmful if swallowed

H314Causes severe skin burns and eye damage

Precautionary statements

P270Do not eat, drink or smoke when using this product.

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

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

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: B99006
Product name: 2-sec-Butylphenol
Purity: 98%
Packaging: 100g
Price: $19.14
Updated: 2024/03/01

TCI Chemical

Product number: B0732
Product name: 2-sec-Butylphenol
Purity: >97.0%(GC)
Packaging: 25g
Price: $30
Updated: 2024/03/01

TCI Chemical

Product number: B0732
Product name: 2-sec-Butylphenol
Purity: >97.0%(GC)
Packaging: 500g
Price: $51
Updated: 2024/03/01

Alfa Aesar

Product number: A18461
Product name: 2-sec-Butylphenol, 98%
Packaging: 250g
Price: $27.65
Updated: 2024/03/01

Alfa Aesar

Product number: A18461
Product name: 2-sec-Butylphenol, 98%
Packaging: 1000g
Price: $64.65
Updated: 2024/03/01

More

Less

2-sec-Butylphenol Chemical Properties,Usage,Production

Chemical Properties

colourless to light yellow liquid

Chemical Properties

The butylphenols include several isomers. Solid butylphenols (28805-86-9) generally have properties similar to the above:

Uses

Chemical intermediate in preparation of resins, plasticizers, surface-active agents.

Uses

Herbicide, Insecticide, Polymerization Inhibitor, Stabilizer Intermediate

Uses

A chemical intermediate in the production of resins, plasticizers, and other products

Definition

ChEBI: A member of the class of phenols that is phenol carrying a butan-2-yl group at position 2.

General Description

Clear colorless liquid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Phenols, such as 2-sec-Butylphenol, do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid.

Hazard

Skin, eye, and upper respiratory tract irri- tant.

Health Hazard

o-sec-Butylphenol is a skin, eye, and respiratory irritant.
Acute occupational exposures have resulted in mild respiratory irritation as well as skin burns.

Fire Hazard

2-sec-Butylphenol is combustible.

Flammability and Explosibility

Not classified

Safety Profile

A poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion and skin contact. A severe skin and eye irritant. Combustible when exposed to heat or flame. To fight fire, use foam, spray, CO2, dry chemical. When heated to decomposition it emits acrid and irritating fumes. See also PHENOL and other butyl phenols

Potential Exposure

Butylphenols may be used as intermediates in manufacturing varnish and lacquer resins; as a germicidal agent in detergent disinfectants; as a pour point depressant, in motor-oil additives; de-emulsifier for oil; soap-antioxidant, plasticizer, fumigant, and insecticide

Shipping

UN2430 Alkylphenols, solid, n.o.s. (including C2-C12 homologues), Hazard class: 8; Labels: 8— Corrosive material

Incompatibilities

Vapors may form explosive mixture with air. These phenol/cresol materials can react with oxidizers; reaction may be violent. Incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may cause the gas to ignite and explode. Heat is also generated by the acid-base reaction with bases; such heating may initiate polymerization of the organic compound. React with boranes, alkalies, aliphatic amines, amides, nitric acid, sulfuric acid. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). These reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid and can explode when heated. Many phenols form metal salts that may be detonated by mild shock

2-sec-Butylphenol Preparation Products And Raw materials

Raw materials

Preparation Products

Fenobucarb

More

Less

2-sec-Butylphenol Suppliers

Americas 1 Belgium 2 Canada 1 China 137 Europe 3 France 2 Germany 5 India 3 Japan 5 Norway 1 Switzerland 2 United Kingdom 7 United States 34 USA 1 Global 204

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

MilliporeSigma (Sigma-Aldrich Corp.)

Tel: --
Fax: --
Email: @sial.com
Country: United States
ProdList: 5414
Advantage: 58

TCI America, Inc. (Tokyo Chemical Industry Co., Ltd.)

Tel: --
Fax: --
Email: .Crew@tcichemicals.com
Country: United States
ProdList: 3164
Advantage: 58

Fluorochem Ltd.

Tel: --
Fax: --
Email: enquiries@fluorochem.co.uk
Country: United States
ProdList: 4583
Advantage: 58

SI GROUP

Tel: --
Fax: --
Email: emea.export@siigroup.com
Country: United States
ProdList: 32
Advantage: 58

Alichem Inc.

Tel: --
Fax: --
Email: sales@alichem.com
Country: United States
ProdList: 6167
Advantage: 58

CALSAK CORPORATION

Tel: --
Fax: --
Email: calsak@calsak.com
Country: United States
ProdList: 430
Advantage: 58

VWR International, LLC.

Tel: --
Fax: --
Email: @sargentwelch.com
Country: United States
ProdList: 6262
Advantage: 58

Penta Manufacturing Company

Tel: --
Fax: --
Email: sales@pentamfg.com
Country: United States
ProdList: 5076
Advantage: 65

Ring Specialty Chemicals Inc.

Tel: --
Fax: --
Email: info@ringchemicals.com
Country: United States
ProdList: 888
Advantage: 39

Spectrum Chemical Mfg. Corp.

Tel: --
Fax: --
Email: marketing@spectrumchemical.com
Country: United States
ProdList: 3113
Advantage: 60

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

Combi-Blocks Inc.

Tel: --
Fax: --
Email: sales@combi-blocks.com
Country: United States
ProdList: 6618
Advantage: 69

SI Group, Inc

Tel: --
Fax: --
Email: customercare3@siigroup.com
Country: United States
ProdList: 659
Advantage: 58

Riedel-de Haen AG

Tel: --
Fax: --
Country: United States
ProdList: 6773
Advantage: 87

Alfa Chemistry

Tel: --
Fax: --
Email: info@Alfa-Chemistry.com
Country: United States
ProdList: 6814
Advantage: 0

Frontier Scientific Services, Inc.

Tel: --
Fax: --
Email: customerservice@frontierssi.com
Country: United States
ProdList: 1575
Advantage: 0

ASDI Incorporated

Tel: --
Fax: --
Email: customerservice@asdi.net
Country: United States
ProdList: 6922
Advantage: 67

HBCChem Inc.

Tel: --
Fax: --
Email: sales@hbcchem-inc.com
Country: United States
ProdList: 4569
Advantage: 30

Ivy Fine Chemicals

Tel: --
Fax: --
Email: sales@ivychem.com
Country: United States
ProdList: 6493
Advantage: 58

Waterstone Technology, LLC

Tel: --
Fax: --
Email: sales@waterstonetech.com
Country: United States
ProdList: 6786
Advantage: 30

Pfaltz & Bauer, Inc.

Tel: --
Fax: --
Email: sales@pfaltzandbauer.com
Country: United States
ProdList: 6828
Advantage: 72

Alfa Aesar

Tel: --
Fax: --
Email: tech@alfa.com
Country: United States
ProdList: 6814
Advantage: 81

3B Scientific Corporation

Tel: --
Fax: --
Email: sales@3bsc.com
Country: United States
ProdList: 6718
Advantage: 47

Aceto Corporation

Tel: --
Fax: --
Email: contact@aceto.com
Country: United States
ProdList: 2619
Advantage: 75

Chemiplus Corporation

Tel: --
Fax: --
Email: okazaki@chemiplus.com
Country: United States
ProdList: 3198
Advantage: 38

SKC Inc.

Tel: --
Fax: --
Email: skcorder@skcinc.com
Country: United States
ProdList: 1378
Advantage: 76

Advance Scientific & Chemical

Tel: --
Fax: --
Email: sales@advance-scientific.com
Country: United States
ProdList: 6419
Advantage: 71

Schenectady International, Inc.

Tel: --
Fax: --
Country: United States
ProdList: 43
Advantage: 75

Spectrum Chemicals & Laboratory Products

Tel: --
Fax: --
Email: sales@spectrumchemical.com
Country: United States
ProdList: 6699
Advantage: 77

MP Biomedicals, Inc.

Tel: --
Fax: --
Country: United States
ProdList: 6561
Advantage: 81

More

Less

View Lastest Price from 2-sec-Butylphenol manufacturers

Career Henan Chemical Co

Product: 2-sec-Butylphenol 89-72-5
Price: US $1.00/KG
Min. Order: 1G
Purity: 98%
Supply Ability: 100KG
Release date: 2018-08-15

89-72-5, 2-sec-ButylphenolRelated Search:

2-Iodophenol 4-Butylphenol Guaiacol 4-tert-Butylcatechol 4-tert-Butylphenol 2-Aminophenol 2-Phenylphenol 2,5-Di(tert-amyl)hydroquinone 2-Nitrophenol BRAZILIN 4-[2,4-Bis(1,1-dimethylpropyl)phenoxy]-1-butanamine THEBAINE 4,6-DINITRO-2-SEC-BUTYLPHENOL, 98+%,2,4-Dinitro-6-sec-butylphenol,4,6-Dinitro-2-sec-butylphenol,4,6-Dinitro-o-sec-butylphenol,dinitro-ortho-sec-butylpheno 2,4-Di-tert-pentylphenol 2,6-DI-SEC-BUTYLPHENOL 4-CHLORO-2-CYCLOHEXYLPHENOL 2-(2,4-Di-tert-pentylphenoxy)butryic acid 2-(1-methylpropyl)phenol，2-sec-buty phenol

OSBP

O-S-BUTYLPHENOL

O-SEC-BUTYLPHENOL

ORTHO-SEC-BUTYLPHENOL

2-SEC-BUTYLPHENOL

1-(1-Methylpropyl)phenol

Phenol, o-sec-butyl-

Phenol,2-(1-methylpropyl)-

Phenol,o-sec-butyl-

2-SEC.-BUTYLPHENOL 98%

O-Sec-Butylphenol,~99%

2-sec-Butylphenol,98%

O-Sec.Butyl Phenol (Osbp)

2-(1-methylpropyl)-pheno

2-(1-Methylpropyl)phenol

2-(1-methylpropyl)-Phenol

2-(2-butyl)phenol

2-sec.Butylfenol

2-sec.butylfenol(czech)

o-sec-butyl-pheno

2-sek.Butylphenol

2-<i>sec</i>-Butylphenol

0-sec-butylphenol

2-sec-Butylphenol &gt

89-72-5

C2H5CHCH3C6H4OH

Organic Building Blocks

Phenols

Oxygen Compounds

Building Blocks

Organic Building Blocks

Oxygen Compounds

Phenols