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60678-73-1

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60678-73-1 Usage

Hydrazine derivative

A compound derived from hydrazine (N2H4) This indicates that 1-tert-butyl-1,2,2-trimethylhydrazine is a modified version of the hydrazine molecule.

Rocket fuel and aerospace propellant

Used in rocket propulsion and aerospace applications This highlights the compound's high energy density and stability, making it suitable for use in rocket fuels and propellants.

High volatility

Easily vaporizes at room temperature This property makes the compound highly volatile, which can contribute to its hazardous nature.

Flammable

Can easily catch fire or explode when exposed to heat or sparks This characteristic increases the risks associated with handling and storing the compound.

Reactive with oxidizing materials

Can react violently with certain chemicals This property poses additional hazards when working with or near other chemicals, especially oxidizers.

Health hazards

Causes irritation to eyes, skin, and respiratory system Exposure to the compound can lead to various health issues, including eye, skin, and respiratory irritation.

Potential organ damage

May have harmful effects on the liver and kidneys Prolonged exposure or ingestion of the compound could lead to damage to vital organs.

Environmental risks

May pose risks to the environment if released into air or water The compound's potential to cause harm to the environment highlights the importance of proper handling and disposal.

Safety precautions

Must be handled and stored with caution and in accordance with safety regulations Due to the various hazards associated with 1-tert-butyl-1,2,2-trimethylhydrazine, it is crucial to follow safety guidelines and regulations when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 60678-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,7 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60678-73:
(7*6)+(6*0)+(5*6)+(4*7)+(3*8)+(2*7)+(1*3)=141
141 % 10 = 1
So 60678-73-1 is a valid CAS Registry Number.

60678-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-tert-butyl-1,2,2-trimethylhydrazine

1.2 Other means of identification

Product number -
Other names Hydrazine,(1,1-dimethylethyl)trimethyl-(9CI)

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:60678-73-1 SDS

60678-73-1Relevant articles and documents

Kinetic Effects of an Unusually Large Neutral to Radical Cation Geometry Change. Slow Electron-Transfer Reactions between Alkylhydrazines

Nelsen, Stephen F.,Rumack, Daniel T.,Meot-Ner (Mautner), Michael

, p. 1373 - 1379 (2007/10/02)

High pressure mass spectrometry was used to measure the kinetics for electron transfer between 54 pairs of tetraalkylhydrazines containing acyclic and f-ve- to seven-membered cyclic and bicyclic rings.Rate constants for electron transfer vary between 18 and 0.03 x 10-11 cm3molecule-1s-1 at 550 K.Variable-temeprature mesuremeants were made on five pairs over a 77-120 deg range.The (Me2N)2(1+), (EtMeN2)2 pair gave Ea=2.7 kcal/mol.The association energy for (Me2N)2 was measured at ΔH0=-13.0 kcal/mol near room temperature.These data are combined to estimate an energy separation of about 15.7 kcal/mol between associated (Me2N)2(1+)/(EtMeN)2 dimer complex and the transition state for electron transfer.The observed Bronsted α value of about 0.5 suggests a large barrier to electron transfer, and the kinetics suggests that the components largely retain their original structures in the associated complex, but that significant distortion is required to reach the transition-state geometry.The effect of alkyl group changes on the electron-transfer rate and comparison of these data with solution experiments are discussed.

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