
Product Name: Direct Yellow 86
C.I. No.: 29325
CAS No.: 50925-42-3
Molecular Formula: C39H30N10Na4O13S4
Molecular Weight:1066.94
Relative Name:
Direct Yellow D-RL,Direct Yellow RL,Direct Fast Yellow D-RL,Direct Fast Yellow D-RLG.
Shade: red light yellow.
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Direct Yellow 86 Physical Properties and light fastness, solubility.
                       Direct Yellow 86 | |
Dyeing depth % | 2 |
Insolubles % | 0.15 |
Light Fastness | 6 |
Washing Fatness | 2-3 |
Rubbing fastness(dry) | 4-5 |
Rubbing fastness(wet) | 3 |
Direct yellow 86 Properties and Applications:
Yellow powder, soluble in water. The high temperature stability is good. Apply to polyester/cotton/polyester sticky, blended fabric dyeing of a bath, especially applicable to a bath dyeing of step, also can used for silk dyeing and paper color.
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Package, 25KG/DRUM, CARTON BOX, BAG
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Note:Â The data contained here are based on our current knowledge and experience. It is the responsibility of user to test our products before the final application.
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The COVID-19 Antigen Saliva Test kit is a lateral flow immunoassay intended for the preliminary screening and qualitative detection of nucleocapsid protein antigen from severe acuterespiratorysyndrome coronavirus SARS-CoV-2which causesthe Coronavirusdisease(COVID-19),in direct saliva sample from individuals suspected of coVD-19 by their healthcare provider within the first seven days of symptom onset.The COVID-19 Antigen Saliva Test kit is for professional use only and is intended to be used as an aid in the diagnosis of SARS CoV-2 infection.
SARS-CoV-2is anenvelopedsingle-stranded RNAvirus ofthe Baenus COVD-19 is an acute respiratory infectious disease. People are generally susceptible.Currently. the patients infected bytheSARS-CoV2are the main source ofinfection:asvmptomatic infected peope car also be an infectious source Based on thecurrentepidemiologica investigation, the incubation period is 1to 14 daysmostly 3to 7 days The main manifestations include feverfatigue and drycough.Nasa congestion, runny nosesore throatmyalgia and diarhea are found in a few cases.
Results are for the identification of SARS-CoV-2 nuceocapsid protein antigen. The SARS-CoV-2 antigen is generally detectable in upper respiratory specimens during the acute phase ofinfectionPositive results indicate the presence of SARS-CoV-2viralantigenshowever cinicai corelation with patient history and other diaanostic information is key to determine status of infection.Positive results don't preclude bacterialinfection or co-infection with other yiruses.eaatveresuts To patients with symptom onset for more than seven days should be treated as presumptive and confirmation with a molecular assayand patient management may be performed according to local regulations as needed.
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