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135-01-3

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135-01-3 Usage

Uses

1,2-Diethylbenzene is used as an intermediate and a building block in organic synthesis. 1,2-Diethylbenzene is used as one of the chemical composition of essential oils from flower and leaf of korean mint.

Synthesis Reference(s)

The Journal of Organic Chemistry, 37, p. 3545, 1972 DOI: 10.1021/jo00795a036

Check Digit Verification of cas no

The CAS Registry Mumber 135-01-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 135-01:
(5*1)+(4*3)+(3*5)+(2*0)+(1*1)=33
33 % 10 = 3
So 135-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14/c1-3-9-7-5-6-8-10(9)4-2/h5-8H,3-4H2,1-2H3

135-01-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L18775)  1,2-Diethylbenzene, 97%   

  • 135-01-3

  • 2g

  • 475.0CNY

  • Detail
  • Alfa Aesar

  • (L18775)  1,2-Diethylbenzene, 97%   

  • 135-01-3

  • 10g

  • 1699.0CNY

  • Detail
  • Alfa Aesar

  • (L18775)  1,2-Diethylbenzene, 97%   

  • 135-01-3

  • 50g

  • 6684.0CNY

  • Detail
  • Aldrich

  • (32008)  1,2-Diethylbenzene  ≥99.0% (GC)

  • 135-01-3

  • 32008-1ML

  • 1,133.73CNY

  • Detail
  • Aldrich

  • (32008)  1,2-Diethylbenzene  ≥99.0% (GC)

  • 135-01-3

  • 32008-5ML

  • 3,918.33CNY

  • Detail
  • Aldrich

  • (D90601)  1,2-Diethylbenzene  technical grade, 92%

  • 135-01-3

  • D90601-5G

  • 1,584.18CNY

  • Detail
  • Aldrich

  • (D90601)  1,2-Diethylbenzene  technical grade, 92%

  • 135-01-3

  • D90601-25G

  • 6,458.40CNY

  • Detail

135-01-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Diethylbenzene

1.2 Other means of identification

Product number -
Other names 1,2-DIETHYLBENZENE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Functional fluids (closed systems),Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:135-01-3 SDS

135-01-3Related news

Assessment of the Developmental Toxicity and Placental Transfer of 1,2-DIETHYLBENZENE (cas 135-01-3) in Rats09/30/2019

Sprague-Dawley rats were administered 1,2-diethylbenzene (1,2-DEB) by gavage on gestational days (GD) 6 through 20 at dose levels of 0 (corn oil), 5, 15, 25 or 35mg/kg. The dams were euthanized on GD21 and the offspring were weighed and examined for external, visceral and skeletal alterations. M...detailed

Bio-distribution study of 1,2-DIETHYLBENZENE (cas 135-01-3) and its main metabolites by whole-body autoradiography and tissue homogenates09/29/2019

The bio-distribution of the neurotoxic 1,2-diethylbenzene (1,2-DEB) was studied in male Sprague-Dawley rats after intravenous administration of [14C] 1,2-DEB (1 mg kg−1). The highest concentrations of [14C] non-volatile metabolites, determined by whole-body auto-radiography, were in the nasal ca...detailed

135-01-3Relevant articles and documents

Seyferth,White

, p. 119,120 (1972)

Method for simultaneously synthesizing methyl-ethylbenzene and diethylbenzene by virtue of one-step method

-

Paragraph 0051-0065, (2016/12/22)

The invention relates to a method for simultaneously synthesizing methyl-ethylbenzene and diethylbenzene by virtue of a one-step method. Ethylene, benzene and methylbenzene are taken as raw materials to perform an alkylation reaction so as to synthesize methyl-ethylbenzene and diethylbenzene in one step. The method comprises a pretreatment stage, a reaction stage and an aftertreatment stage. In the method, one reaction system is adopted, and alkylation reaction and aftertreatment are sequentially performed so as to separate components, so that target products are obtained, and thus one-step simultaneous synthesis of methyl-ethylbenzene and diethylbenzene is realized; the problem that two independent devices are respectively used for production in a traditional production process is avoided, and the whole reaction process is convenient and rapid; the yields of different components can be effectively adjusted by adjusting different proportions of raw materials, and unreacted benzene and methylbenzene and the ethylbenzene generated in a reaction process are separated and recycled to serve as raw materials once again, so that the production cost is greatly saved, and meanwhile, the method can adapt to variations of the market to the greatest extent.

Synthesis, characterization and application of MCM-22 zeolites via a conventional HMI route and temperature-controlled phase transfer hydrothermal synthesis

Xing, Enhui,Shi, Yanchun,Xie, Wenhua,Zhang, Fengmei,Mu, Xuhong,Shu, Xingtian

, p. 8514 - 8522 (2015/03/05)

With less environmental and economical impact, temperature-controlled phase transfer hydrothermal synthesis of MWW zeolites was realized with hexamethyleneimine as a structure-directing agent and aniline as a structure-promoting agent. MCM-22 zeolite, synthesized via temperature-controlled phase transfer hydrothermal synthesis, is nearly identical concerning chemical composition and structure, and possesses nearly identical properties with respect to porosity, Si/Al ratio, thermal behavior and catalytic activity at 200°C, compared with that made from conventional synthesis with hexamethyleneimine as the only template.

Size-controlled synthesis of MCM-49 zeolites and their application in liquid-phase alkylation of benzene with ethylene

Shi, Yanchun,Xing, Enhui,Xie, Wenhua,Zhang, Fengmei,Mu, Xuhong,Shu, Xingtian

, p. 13420 - 13429 (2015/02/19)

Size-controlled synthesis of MCM-49 zeolites was achieved via topology reconstruction from NaY zeolites with different sizes. SEM images showed that the sizes of the reconstructed H-MCM-49 zeolites were controlled by those of the parent NaY zeolites. Smal

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