CRJ042-1-TH Datasheet

CUI DEVICES
date 04/05/2021
page 1 of 3
cuidevices.com
MODEL: CRJ042-1-TH │ DESCRIPTION: MODULAR JACK
FEATURES
• 8P8C (RJ45)
• keyed
• gold over nickel plating
• through hole
SPECIFICATIONS
parameter conditions/description min typ max units
rated voltage 150 Vac
rated current 1.5 A
withstanding voltage for 1 minute 1,500 Vac
contact resistance 40 mΩ
insulation resistance 500 MΩ
insertion/withdrawal force 6.12 kgf
operating temperature 0 70 °C
storage temperature -40 80 °C
life 1,000 cycles
flammability rating UL94V-0
RoHS yes
packaging
carton size: 400 x 303 x 258 mm
tray QTY: 100 pcs per tray
carton QTY: 2,600 pcs per carton
SOLDERABILITY
parameter conditions/description min typ max units
wave soldering for maximum 5 seconds 240 °C
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CUI Devices │ MODEL: CRJ042-1-TH │ DESCRIPTION: MODULAR JACK date 04/05/2021│ page 2 of 3
MECHANICAL DRAWING
ITEM DESCRIPTION MATERIAL PLATING/COLOR
1 insulator PBT (UL94V-0) black
2contact
terminals phosphor bronze
contact area: 6 µ”
gold over nickel
solder area: tin over
nickel
3 shield brass nickel
Recommended PCB Layout
Top View
units: mm
tolerance:
X ±0.5 mm
X.X ±0.38 mm
X.XX ±0.25 mm
X.XXX ±0.10 mm
PCB: ±0.05 mm
PCB thickness: 1.6 mm
unless otherwise noted
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CUI DEVICES
CUI Devices │ MODEL: CRJ042-1-TH │ DESCRIPTION: MODULAR JACK date 04/05/2021│ page 3 of 3
cuidevices.com
CUI Devices offers a one (1) year limited warranty. Complete warranty information is listed on our website.
CUI Devices reserves the right to make changes to the product at any time without notice. Information provided by CUI Devices is believed to be accurate and reliable. However, no
responsibility is assumed by CUI Devices for its use, nor for any infringements of patents or other rights of third parties which may result from its use.
CUI Devices products are not authorized or warranted for use as critical components in equipment that requires an extremely high level of reliability. A critical component is any
component of a life support device or system whose failure to perform can be reasonably expected to cause the failure of the life support device or system, or to affect its safety or
effectiveness.
rev. description date
1.0 initial release 04/05/2021
The revision history provided is for informational purposes only and is believed to be accurate.
REVISION HISTORY
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