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(dipropan-2-ylamino)[(2,3,3-trichloroprop-2-en-1-yl)sulfinyl]methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71133-38-5

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71133-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71133-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,3 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71133-38:
(7*7)+(6*1)+(5*1)+(4*3)+(3*3)+(2*3)+(1*8)=95
95 % 10 = 5
So 71133-38-5 is a valid CAS Registry Number.

71133-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 16,16-dimethylheptadecan-1-amine

1.2 Other means of identification

Product number -
Other names EINECS 273-280-7

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:71133-38-5 SDS

71133-38-5Upstream product

71133-38-5Downstream Products

71133-38-5Relevant academic research and scientific papers

Fatty acid and wax biosynthesis in susceptible and triallate-resistant Avena fatua L.

Kern,Jackson,Dyer

, p. 21 - 26 (2007/10/03)

The recent characterization of triallate-resistant lines of wild oat (Arena fatua L.) deficient in triallate sulfoxidation provides an experimental system to investigate and differentiate the effects of triallate and triallate sulfoxide on wax and lipid biosynthesis. Greenhouse applications of triallate dramatically reduced epicuticular wax deposition in susceptible (s) but not resistant (R) wild oats. Triallate treatment had no effect on in-vivo concentrations of C12 to C26 fatty acids and fatty alcohols in R plants, while elongated fatty acid fractions (C > 18) were significantly reduced in S plants. In contrast, treatment with triallate sulfoxide reduced in-vivo concentrations of elongated fatty acids equally in R and S, supporting the hypothesis that triallate sulfoxide is more inhibitory than triallate towards fatty acid elongases. Although de-novo synthesis of short-chain fatty acids was not affected by triallate or triallate sulfoxide in R or S plants, synthesis of elongated fatty acid fractions was dramatically reduced in S plants by triallate. Fatty acid biosynthesis in R and S plants was equally sensitive to triallate sulfoxide. The results support the idea that in-vivo triallate sulfoxidation is necessary for herbicidal activity, and confirm that reduced rates of triallate sulfoxidation confer resistance in R wild oats.

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