CD4053BCM Fairchild Semiconductor, CD4053BCM Datasheet - Page 13

• Manufacturer Part Number: CD4053BCM
• Description: IC MUX/DEMUX TRIPLE 2X1 16SOIC
• Manufacturer: Fairchild Semiconductor
• Series: 4000Br

Specifications of CD4053BCM

• Function: Multiplexer/Demultiplexer
• Circuit: 3 x 2:1
• On-state Resistance: 240 Ohm
• Voltage Supply Source: Dual Supply
• Voltage - Supply, Single/dual (±): ±5 V ~ 15 V
• Current - Supply: 20µA
• Operating Temperature: -55°C ~ 125°C
• Mounting Type: Surface Mount
• Package / Case: 16-SOIC (0.154", 3.90mm Width)
• Number Of Channels: 3 Channel
• On Resistance (max): 1050 Ohms
• Propagation Delay Time: 55 ns
• On Time (max): 1200 ns
• Off Time (max): 420 ns
• Supply Voltage (max): 15 V
• Supply Voltage (min): 5 V
• Maximum Power Dissipation: 500 mW
• Maximum Operating Temperature: + 125 C
• Minimum Operating Temperature: - 55 C
• Mounting Style: SMD/SMT
• Number Of Switches: 3
• Lead Free Status / RoHS Status: Lead free / RoHS Compliant

Physical Dimensions
Fairchild does not assume any responsibility for use of any circuitry described, no circuit patent licenses are implied and
Fairchild reserves the right at any time without notice to change said circuitry and specifications.
LIFE SUPPORT POLICY
FAIRCHILD’S PRODUCTS ARE NOT AUTHORIZED FOR USE AS CRITICAL COMPONENTS IN LIFE SUPPORT
DEVICES OR SYSTEMS WITHOUT THE EXPRESS WRITTEN APPROVAL OF THE PRESIDENT OF FAIRCHILD
SEMICONDUCTOR CORPORATION. As used herein:
1. Life support devices or systems are devices or systems
which, (a) are intended for surgical implant into the
body, or (b) support or sustain life, and (c) whose failure
to perform when properly used in accordance with
instructions for use provided in the labeling, can be rea-
sonably expected to result in a significant injury to the
user.
16-Lead Plastic Dual-In-Line Package (PDIP), JEDEC MS-001, 0.300 Wide
inches (millimeters) unless otherwise noted (Continued)
Package Number N16E
13
2. A critical component in any component of a life support
device or system whose failure to perform can be rea-
sonably expected to cause the failure of the life support
device or system, or to affect its safety or effectiveness.
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