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sec-Butyllithium

sec-Butyllithium Suppliers list
Company Name: Lianyungang Jiezhong Pharmaceutical Technology Co., Ltd  Gold
Tel: 13165449089
Email: 2124455948@qq.com
Company Name: Huangshi Bo’Er Chemical Co., Ltd.  Gold
Tel: 0714-6401888 18671400300
Email: 273568016@qq.com
Company Name: ZhengZhou HuaWen Chemical Co.Ltd  Gold
Tel: 0370-2785118 17550508557
Email: 675141927@qq.com
Company Name: J & K SCIENTIFIC LTD.  Gold
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com

sec-Butyllithium manufacturers

  • SEC-BUTYLLITHIUM
  • SEC-BUTYLLITHIUM pictures
  • $30.00
  • 2025-06-27
  • CAS:598-30-1
  • Min. Order: 50KG
  • Purity: 99%
  • Supply Ability: 500000kg
  • SEC-BUTYLLITHIUM
  • SEC-BUTYLLITHIUM pictures
  • 2025-06-20
  • CAS:598-30-1
  • Min. Order: 1kg
  • Purity: 0.99
  • Supply Ability: 10 tons
sec-Butyllithium Basic information
Product Name:sec-Butyllithium
Synonyms:sec-Butyllithium, 1.0 M solution in Hexane, HySeal;S-BUTYLLITHIUM;LITHIUM-2-BUTANIDE;LITHIUM SEC-BUTYL;s-butyllithium(1.3M)in cyclonexane;Sec-butyllithium 1.4M in cyclohexane;sec-ButyllithiuM, 12% (ca 1.4M) in cyclohexane/hexane, packed in resealable septuM seal bottle;sec-ButyllithiuM, 1.3 M solution in Cyclohexane/hexane, SpcSeal
CAS:598-30-1
MF:C4H9Li
MW:64.06
EINECS:209-927-7
Product Categories:straight chain compounds;Ionic Polymerization Initiators;25mL Sure/Seal Reagents;Alkyl;Chemical Synthesis;Materials Science;Organic Bases;Organolithium;Organometallic Reagents;Polymer Science;Polymerization Initiators;Reagents for Polymerization;Synthetic Reagents;metal alkyl
Mol File:598-30-1.mol
sec-Butyllithium Structure
sec-Butyllithium Chemical Properties
density 0.769 g/mL at 25 °C
Fp 1 °F
storage temp. 2-8°C
form Liquid
color Clear colorless
Sensitive Air & Moisture Sensitive
BRN 3587206
Exposure limitsACGIH: TWA 100 ppm
OSHA: TWA 300 ppm(1050 mg/m3)
NIOSH: IDLH 1300 ppm; TWA 300 ppm(1050 mg/m3)
InChIInChI=1S/C4H9.Li/c1-3-4-2;/h3H,4H2,1-2H3;
InChIKeyVATDYQWILMGLEW-UHFFFAOYSA-N
SMILESC(C)([Li])CC
CAS DataBase Reference598-30-1(CAS DataBase Reference)
EPA Substance Registry SystemLithium, (1-methylpropyl)- (598-30-1)
Safety Information
Hazard Codes F,C,N
Risk Statements 11-15-17-34-50/53-65-67-66-51/53-14/15
Safety Statements 26-36/37/39-43-45-60-61-62-33-16
RIDADR UN 3394 4.2/PG 1
WGK Germany 2
1-10
TSCA TSCA listed
HazardClass 4.3
PackingGroup I
HS Code 29319090
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
sec-Butyllithium Usage And Synthesis
Descriptionsec-Butyllithium. [598-30-1], sec-C4H9Li, Mr 64.06, is a spontaneously flammable, colorless, viscous liquid that forms tetramers in hydrocarbon solvents. It is commercially available only as 12 % solution in cyclohexane and methylcyclohexane. sec-Butyllithium is more nucleophilic and decomposes more readily than n-butyllithium. A 12 % solutionin cyclohexane at 20 ℃ undergoesthermal decomposition to the extent of 1.4 % of the active material per month. The thermal decomposition yields butene gas and LiH; the latter is insoluble and responsible for the increasing turbidity of secbutyllithium solutions on prolonged storage. Therefore solutions of sec-butyllithium must be kept cool during storage and transportation.
Chemical Propertiessec-Butyllithium is a colorless crystalline solid or clear yellowish solution. It is more reactive than n-butyllithium. Its solutions are unstable and decompose about 10 to 15 times as fast as n-butyllithium under the same conditions.
sec-Butyllithium
Usessec-Butyllithium is used almost exclusively as a polymerization catalyst. It is more expensive than n-butyllithium and is used mainly because of its greater reactivity and faster polymerization initiation.
Preparationsec-Butyllithium is produced by the reaction of sec-butyl chloride with lithium metal dispersion in hydrocarbon solvents. The lithium metal should contain catalytic amounts of up to 2 % sodium metal to attain a rapid reaction with the chloride and to minimize coupling. Massive substitution of sodium metal for lithium metal as is done in the preparation of n-butyllithium results in lower yields. Isopentane, hexane and cyclohexahe are typical solvents. Industrial and laboratory preparations are similar.
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