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L-Tryptophan(CAS# 73-22-3)

Chemical Property:

Molecular Formula C11H12N2O2
Molar Mass 204.23
Density 1.34
Melting Point 289-290°C (dec.)(lit.)
Boling Point 342.72°C (rough estimate)
Specific Rotation(α) -31.1 º (c=1, H20)
Flash Point 224.7°C
Water Solubility 11.4 g/L (25 ºC)
Solubility Slightly soluble in water (1.14%, 25°C), hardly soluble in ethanol. Soluble in dilute acid or base.
Vapor Presure 8.3E-09mmHg at 25°C
Appearance Crystalline powder
Color White to yellow-white
Merck 14,9797
BRN 86197
pKa 2.46(at 25℃)
PH 5.5-7.0 (10g/l, H2O, 20℃)
Storage Condition 2-8°C
Stability Stable. Incompatible with strong acids, strong oxidizing agents.
Sensitive Sensitive to light
Refractive Index -32 ° (C=1, H2O)
MDL MFCD00064340
Physical and Chemical Properties density 1.34
melting point 280-285°C
specific optical rotation -31.1 ° (c = 1, H20)
water-soluble 11.4g/L (25°C)
Use Improve nutrition, enhance physical fitness.

Product Detail

Product Tags

Hazard Symbols Xi – Irritant
Risk Codes R33 – Danger of cumulative effects
R40 – Limited evidence of a carcinogenic effect
R62 – Possible risk of impaired fertility
R41 – Risk of serious damage to eyes
R37/38 – Irritating to respiratory system and skin.
R36/37/38 – Irritating to eyes, respiratory system and skin.
R22 – Harmful if swallowed
Safety Description S24/25 – Avoid contact with skin and eyes.
S36/37/39 – Wear suitable protective clothing, gloves and eye/face protection.
S36 – Wear suitable protective clothing.
S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany 2
RTECS YN6130000
FLUKA BRAND F CODES 8
TSCA Yes
HS Code 29339990
Toxicity LD508mmol / kg (rat, intraperitoneal injection). It is safe when used in food (FDA, §172.320, 2000).

 

Introduction

L-Tryptophan is a chiral amino acid with an indole ring and an amino group in its structure. It is usually a white or yellowish crystalline powder that is slightly soluble in water and has increased solubility under acidic conditions. L-tryptophan is one of the essential amino acids that cannot be synthesized by the human body, is a component of proteins, and is also an indispensable raw material in the synthesis and metabolism of proteins.

 

There are two main ways to prepare L-tryptophan. One is extracted from natural sources, such as animal bones, dairy products, and plant seeds. The other is synthesized by biochemical synthesis methods, using microorganisms or genetic engineering technology for synthesis.

 

L-tryptophan is generally safe, but excessive intake may have some side effects. Excessive intake may cause gastrointestinal upset, nausea, vomiting, and other digestive reactions. For certain patients, such as those with rare hereditary tryptophan in the disease, ingestion of L-tryptophan may trigger more serious health problems.


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