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1,1,1,3,4-Pentachlorobutane is a chlorinated hydrocarbon with the chemical formula C4H5Cl5. It is a colorless liquid with a pungent odor and is known for its high boiling point and low solubility in water. 1,1,1,3,4-Pentachlorobutane is primarily used as a solvent, particularly in the production of chlorinated rubber and as a fire retardant. Due to its persistence in the environment and potential health risks, including its classification as a probable human carcinogen, its production and use have been significantly reduced or banned in many countries.

1071-08-5

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1071-08-5 Usage

Type

Synthetic chemical compound

Composition

Five chlorine atoms attached to a butane molecule

Physical State

Non-flammable, colorless liquid

Odor

Pungent

Primary Uses

a. Intermediate in the production of chemicals (pharmaceuticals, agricultural products)
b. Solvent
c. Manufacturing of plastics and rubber

Hazardous Classification

Harmful if inhaled, swallowed, or absorbed through the skin

Health Effects

a. Respiratory irritation
b. Skin irritation
c. Long-term health effects (liver and kidney damage)

Safety Precautions

Strict safety measures should be followed when handling and using 1,1,1,3,4-Pentachlorobutane

Check Digit Verification of cas no

The CAS Registry Mumber 1071-08-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1071-08:
(6*1)+(5*0)+(4*7)+(3*1)+(2*0)+(1*8)=45
45 % 10 = 5
So 1071-08-5 is a valid CAS Registry Number.

1071-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,3,4-pentachlorobutane

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:1071-08-5 SDS

1071-08-5Downstream Products

1071-08-5Relevant academic research and scientific papers

The Reaction of Polyhalides with Allylsilanes Catalyzed by Copper(I) Chloride

Mitani, Michiharu,Hujita, Shigenori

, p. 3055 - 3060 (2007/10/03)

Allyltrimethylsilane reacted with polyhalogen compounds in the presence of copper species, such as copper(I) chloride, copper(II) chloride or metallic copper, to form polyhalo compounds containing an allyl group. Other allylsilane derivatives than allyltrimethylsilane were also subjected to a reaction with carbon tetrachloride. 3-Chloro- or 3-bromo-3-trimethylsilyl-1-propene gave 4,4,4-trichloro-1-trimethylsilyl-1-butene. Ethyl 1-trimethylsilylallyl carbonate afforded ethyl 4,4,4-trichloro-1-butenyl carbonate along with a hydrotrichloromethylation product. 2-Methyl-3-trimethylsilyl-1-propene yielded a product based on the addition of a trichloromethyl group followed by hydrogen-elimination from a 2-methyl group.

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