| Name | Sodium hyaluronate |
|---|---|
| Synonyms |
SODIUM HYALURONATE INJECTABLE ADE LMW
HYALURONIC ACID SODIUM FROM ROOSTER*COMB Sodium Hyaluronate(HA) HYALURONIC ACID SODIUM FROM*STRTOCOCCU S ZOOIDEM Hyaluronic acid sodium salt from Strtococcus Sph HYALURONIC ACID SODIUM SALT FROM ROO hyaluronic acid sodium salt from human umbilical cord hyaluronic SODIUM HYALURONATE OPHTHALMIC ADE MMW SODIUM HYALURONATE COSMETIC ADE LMW SODIUM HYALURONATE PHMACEUTICAL ADE (MMW) SODIUM HYALURONATE COSMETIC ADE HMW HYALURONIC ACID - FOOD hyaluronic acid sodium salt HYALURONIC ACID ADE B ( HA-Q ) Hyaluronic acid-Na-salt from rooster comb HYALURONIC ACID INJECTABLE cockscomb Si-4402 SODIUM HYALURONATE(TOPICAL ADE) Hyaluronesodium Hyaluronate Sodium [USAN:JAN] hyaluronic acid sodium salt from strtococcus equi Food ade SodiuM hyaluronate Hyasis 850P HYALURONIC ACID LOW ENDOTOXIN Hyaluronate HYALURONIC ACID - COSMETIC HYALURONIC ACID LOW MOL (10,000) hyaluronic acid sodium salt from strtococcus zooidemicus Hyaluronic Acid Sodium Salt from Cockscomb HYALURONIC ACID HA-L510 PF SODIUM HYALURONATE PHMACEUTICAL ADE (HMW) HYALURONIC ACID ADE A ( HA-QSS ) EINECS 232-678-0 MFCD00875848 SODIUM HYALURONATE COSMETIC ADE MMW SODIUM HYALURONATE OPHTHALMIC ADE LMW Sl-1010 HYALURONIC ACID SODIUM SALT 2,000,00 HYALURONIC ACID SODIUM SALT F. STRTO-C OCCUS EQUI SP Sodium 4-O-(2-acetamido-2,3-dideoxy-β-D-ribo-hexopyranosyl)-β-D-glucopyranuronate SODIUM HYALURONATE OPHTHALMIC ADE HMW SODIUM HYALURONATE INTRATICULADE HMW Injection ade SodiuM hyaluronate β-Sodium glucuronate-(1,3)-β-N-acetyl-D-glucosamine HYALURONIC ACID SODIUM SALT 8 Medical ade SodiuM hyaluronate Hyaluronic Acid Sodium Salt from Microorganism HYALURONIC ACID - EYE DROP HYALURONIC ACID SODIUM SALT FROM STR SODIUM HYALURONATE SOLUTION HYALURONIC ACID - INJECTION Poly(β-glucuronic acid-[1→3]-β-N-acetylglucosamine-[1→4]), alternating Sodium hyaluronate HYALURONIC ACID LMW hyaluronic acid sodium salt from rooster comb Chlamyhyaluronic acid sodium salt SODIUMHYALURINATE SODIUM HYALURONATE PHMACEUTICAL ADE (LMW) β-D-Glucopyranuronic acid, 4-O-[2-(acetylamino)-2,3-dideoxy-β-D-ribo-hexopyranosyl]-, sodium salt (1:1) alternating copoly(β-glucuronic acid-[1→3]-β-n-acetylglucosamine-[1→4]) HYALURONIC ACID EYE DROPS |
| Description | Hyaluronic acid sodium salt is a biopolymer composed of repeating units of disaccharides with various applications. |
|---|---|
| Related Catalog | |
| In Vitro | Hyaluronic acid (HA) is widely used in aesthetic medicine due to its binding ability with a large number of water molecules. It improves tissue hydration and their resistance to mechanical damage. HA plays an important role in wound healing, ovulation, fertilization, signal transduction, and tumor physiology. HA is used in joint diseases such as osteoarthritis or rheumatoid arthritis. HA of a high molecular mass reduces the chemotaxis and migration of inflammatory cells which acts as a good barrier to the inflammatory process and protects against the effects of free radicals. HA is used in ophthalmology due to its lubricating properties for the corneal endothelium, and improves tissue hydration and cellular resistance to mechanical damage in aesthetic dermatology, and has marginal adverse effects. Several trials indicate its role in tumor markers, liver diseases, and in pharmaceuticals[1]. Hyaluronan plays an important role in cancer growth and metastasis. HA and HA fragment-tumor cell interaction could activate the downstream signaling pathways, promoting cell proliferation, adhesion, migration and invasion, and inducing angiogenesis, lymphangiogenesis, epithelial-mesenchymal transition, stem cell-like property, and chemoradioresistance in digestive cancers[2]. |
| In Vivo | The impact of applied intra-articular HA has been proven in many studies in animals. Studies on HA have shown that it promotes the synthesis of cartilage matrix, prevents its degradation, reduces inflammation, stimulates the synthesis of endogenous HA, and improves the resilience and moisture of cartilage[1]. High molecular size HA preparations, applied topically, promote healing of fresh skin wounds. They also promote the healing of venous leg ulcers and are useful in the management of chronic wounds[3]. |
| References |
[2]. Wu RL, et al. Hyaluronic acid in digestive cancers. J Cancer Res Clin Oncol. 2017 Jan;143(1):1-16. |
| Density | 1.78g/cm3 |
|---|---|
| Boiling Point | 791.6ºC |
| Molecular Formula | C14H22NNaO11 |
| Molecular Weight | 799.63800 |
| Flash Point | 432.5ºC |
| Exact Mass | 799.22300 |
| PSA | 399.71000 |
| Storage condition | −20°C |
| Stability | Stable. Incompatible with strong oxidizing agents. |
| Water Solubility | SOLUBLE |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
|---|---|
| Hazard Codes | Xi: Irritant; |
| Risk Phrases | 36/37/38 |
| Safety Phrases | 22-24/25-36/37/39-27-26 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| RTECS | MT7250000 |
| HS Code | 3913900000 |
|
~%
9067-32-7 |
| Literature: WO2005/16341 A1, ; Page/Page column 3 ; |
| HS Code | 3913900000 |
|---|