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63737-71-3

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63737-71-3 Usage

Description

N,N'-DIISOPROPYL-1,3-PROPANEDIAMINE is a diamine compound characterized by the presence of two isopropyl groups attached to the nitrogen atoms of the amine functional groups. It is primarily utilized as a catalyst in various industrial processes, particularly in the production of polyurethane foams and resins. This chemical is appreciated for its ability to facilitate the formation of polyurethane polymers with favorable physical and chemical properties. Moreover, it is recognized for its low toxicity and relatively low volatility, which makes it a safer alternative to other catalysts in industrial applications. N,N'-DIISOPROPYL-1,3-PROPANEDIAMINE is instrumental in the synthesis of polyurethane materials for a diverse array of industrial and consumer products.

Uses

Used in the Polyurethane Industry:
N,N'-DIISOPROPYL-1,3-PROPANEDIAMINE is used as a catalyst for the production of polyurethane foams and resins. It plays a vital role in promoting the formation of polyurethane polymers with desirable physical and chemical properties, which are essential for creating high-quality end products.
Used in Industrial Applications:
N,N'-DIISOPROPYL-1,3-PROPANEDIAMINE is used as a catalyst in various industrial processes to enhance the synthesis of polyurethane materials. Its low toxicity and low volatility make it a safer option for these applications, reducing the risk of harmful exposure to workers and the environment.
Used in Consumer Product Manufacturing:
N,N'-DIISOPROPYL-1,3-PROPANEDIAMINE contributes to the production of a wide range of consumer products that incorporate polyurethane materials. Its role in the synthesis of these materials ensures that the final products possess the necessary qualities for their intended uses, such as durability, flexibility, and resistance to wear and tear.

Check Digit Verification of cas no

The CAS Registry Mumber 63737-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,3 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63737-71:
(7*6)+(6*3)+(5*7)+(4*3)+(3*7)+(2*7)+(1*1)=143
143 % 10 = 3
So 63737-71-3 is a valid CAS Registry Number.

63737-71-3 Well-known Company Product Price

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  • Aldrich

  • (332542)  N,N′-Diisopropyl-1,3-propanediamine  96%

  • 63737-71-3

  • 332542-5G

  • 1,356.03CNY

  • Detail

63737-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-di(propan-2-yl)propane-1,3-diamine

1.2 Other means of identification

Product number -
Other names N,N'-bis(1'-methylethyl)-1,3-propanediamine

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:63737-71-3 SDS

63737-71-3Relevant articles and documents

Carbanion-Accelerated Claisen Rearrangements. 8. Phosphonamide Anion-Stabilizing Groups

Denmark, Scott E.,Stadler, Heinz,Dorow, Roberta L.,Kim, Jung-Ho

, p. 5063 - 5079 (2007/10/02)

The utility of various phosphonamide groups has been examined in the context of the carbanion-accelerated Claisen rearrangement (CACR).An extensive survey has identified the N,N'-dibenzyl-1,3,2-diazaphospholidine group 11 to be optimal in the ease of construction of the CACR precursors and the facility and stereoselectivity of the rearrangement.Using n-butyllithium as the base, the phosphonamides rearranged readily at -20 deg C with complete regioselectivity and in good yield (74-79percent).The phosphonates also showed a high level of diastereoselectivity (>95percent de) but the yield from the (Z)-2-butenyl precursor (anti product) was only 45percent.A chiral N,N'-dibenzyl-1,3,2-diazaphospholidine 12 derived from trans-1,2-cyclohexanediamine was examined.Although the CACR proceeded very cleanly (71-85percent) and with high internal selectivity (94percent de), the relative asymmetric induction was poor (16-20percent de).This was also the case for a chiral N,N'-dibenzyl-1,3,2-diazaphosphorinane 15 derived from (R,R)-1,3-diphenyl-1,3-propanediamine and N,N'-dibenzyl-1,3,2-diazaphosphepine 16 derived from 6,6'-dimethyl-2,2'-diaminobiphenyl.The characteristic features of the CACR were compared with the aryl sulfone and phosphonate versions.

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