Bilirubin CAS#635-65-4

CAS Number: 635-65-4
Chemical Formula: C33H36N4O6
Synonyms:

(Z,Z)-Bilirubin
Biline-8,12-dipropionic acid, 1,10,19,22,23,24-hexahydro-2,7,13,17-tetramethyl-1,19-dioxo-3,18-divinyl-
Cholerythrin

Appearance: Orange Red Powder

MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)

Contact Now E-Mail Telephone WhatsApp

Product Details

Bilirubin CAS#635-65-4

Bilirubin is a yellow breakdown product of heme catabolism, formed when heme is cleaved by heme oxygenase. This reaction produces carbon monoxide and biliverdin, which is rapidly reduced to bilirubin by biliverdin reductase. Bilirubin has key roles as a free radical scavenger with antioxidant and anti-inflammatory actions. Free and albumin-bound bilirubin can also scavenge nitric oxide (NO) and NO-related species. Unconjugated bilirubin is highly water-insoluble and must be conjugated with glucuronides to become water soluble and subsequently excreted by the liver and kidney.

Bilirubin Chemical Properties

Melting point	192 °C
Boiling point	641.7°C (rough estimate)
density	1.2163 (rough estimate)
refractive index	1.6000 (estimate)
storage temp.	-20°C
solubility	aqueous acid: soluble
form	powder
pKa	4.62±0.10(Predicted)
color	orange
Water Solubility	practically insoluble
Sensitive	Light Sensitive
Merck	14,1218
BRN	74376
Stability:	Stable. Refrigerate.
Cosmetics Ingredients Functions	CHELATING REDUCING ANTIOXIDANT
InChIKey	BPYKTIZUTYGOLE-IFADSCNNSA-N
SMILES	CC1=C(C=C)\C(NC1=O)=C\c2[nH]c(Cc3[nH]c(\C=C4/NC(=O)C(C=C)=C4C)c(C)c3CCC(O)=O)c(CCC(O)=O)c2C
EPA Substance Registry System	Bilirubin (635-65-4)

Safety Information

Hazard Codes	Xn
Risk Statements	62-36/37/38-20/21/22
Safety Statements	22-24/25-36-26
WGK Germany	2
RTECS	DU3038000
F	8
TSCA	TSCA listed
HS Code	29339990
Storage Class	11 - Combustible Solids

Product Application Of Bilirubin CAS#635-65-4

Bilirubin is widely utilized to monitor the liver function and their disease, such as hepatitis or cirrhosis; or the effects of medicines which are damage the liver. It acts as a pigment in certain algae to capture light energy. Its double bonds are isomerizes in the presence of light, which is employed in phototherapy of jaundiced newborns babies. It is used to detect the blocking in bile ducts.

Fact Factory and Equipment Show

Gardenia Yellow#94238-00-3